Welcome to the call. Fiscal 2021 was an extraordinary year for the entire world and for Catalent. During the year, we achieved truly significant results financially, operationally, and in terms of making a meaningful impact on our global community, including accelerating our capacity expansions and infrastructure, substantially expanding and deepening one of the best talent pools in the industry, intensifying our longstanding commitment to sustainable practices, and accelerating our growth strategy, all while delivering record financial results. We rose to the challenge of scaling our capacity to meet significant demand for vaccines and treatments to address the COVID-19 pandemic, and are on track to deliver well over 1 billion COVID-19 vaccine doses this calendar year. We've also continued to develop and manufacture a broad range of other important medicines under difficult, unprecedented, and rapidly changing global conditions. Our top priority throughout the pandemic has been to keep our employees safe, and we continue to be humbled by the dedication of the more than 17,000 members of our team around the world who have enabled us to grow the company and deliver for our customers and their patients during this tumultuous time. Through our shared experience navigating this pandemic, we've grown as individuals and as a company, added substantial new capabilities, and strengthened partnerships that together enhance our ability to continue to develop and deliver products that help people live better, healthier lives. With that overview, I'll now provide a summary of our financials for the fourth quarter and full fiscal year, as well as operational highlights since our last earnings call. I'll then conclude my prepared remarks with an overview of the acquisition of Bettera Wellness, which we announced this morning. Our net revenue for the fourth quarter was $1.19 billion, increasing 25% as reported, or 22% in constant currency compared to the fourth quarter of fiscal 2020. When excluding acquisitions as well as the divesture of our Blow-Fill-Seal business, which closed in March, organic growth was 26% measured in constant currency. Our adjusted EBITDA of $348 million for the fourth quarter increased 30% as reported, or 27% in constant currency compared to the fourth quarter of fiscal 2020, which includes organic growth of 32% measured in constant currency. Our adjusted net income for the fourth quarter was $209 million, or $1.16 per diluted share, up from $0.90 per diluted share in the corresponding prior year period. The Biologics segment, given the continued high demand for drug products, drug substance, and viral-based offerings, was again the top contributor to Catalent's financial performance, with organic revenue growth of 66% and segment EBITDA more than doubling from the fourth quarter of last year. Our Softgel and Oral Technologies segment continued to experience some of the same pandemic-related headwinds in the fourth quarter, with net revenue down 1% over the fourth quarter of last year on a constant currency basis. Margins improved year-over-year, and so is our outlook, as we're seeing business gradually come back and we expect to return to organic growth in fiscal 2022. Our Oral & Specialty Delivery segment had organic net revenue growth in the mid-teens after excluding the results due to the product in our respiratory platform that we voluntarily recalled last September. In OSD, like SOT, we're also seeing that certain offerings within that segment impacted by the pandemic are beginning to come back. Finally, our Clinical Supply Services segment posted over 20% constant currency net revenue growth and strong margin compared to the fourth quarter of fiscal 2020, a comparison period that included widespread disruption to clinical trials during global lockdowns as a result of the pandemic. For our full fiscal 2021, net revenue and adjusted EBITDA came in at record levels, driven by robust growth in our Biologics business, which represented 48% of our net revenue in the year. Fiscal 2021 net revenue was $4 billion and constant currency organic growth was 25% compared to the prior fiscal year. We estimate approximately 18 percentage points or more than $550 million of our organic growth last year was derived from the net impact of the COVID-19 pandemic, after factoring in the amount of net revenue generated from COVID-19 projects against opportunity costs and pandemic-related headwinds that were created in some of our service offerings. Adjusted EBITDA exceeded $1 billion, resulting in constant currency organic growth of 32% compared to fiscal 2020. We also increased our adjusted EBITDA margin to 25.5%, up 120 basis points from the 24.3% adjusted EBITDA margin in fiscal 2020. To meet our commitments to our customers and their patients, a number of Catalent facilities have been operating 24 hours a day, seven days a week for more than a year. At the same time, we've increased our workforce from 14,000 at the end of the last fiscal year to more than 17,000 today to meet our growing production volume. As we've said on past calls, COVID-19 has not only accelerated our strategic plans, but also accelerated returns on the strategic investments we've made, enabling us to put additional cash to work to continue to drive our long-term growth. Let me update you on some of these capacity and capability investments. As you know, our 950,000 sq ft facility in Bloomington, Indiana, plays a critical role in the global vaccine production effort. Over the last year, we've brought online two new vial filling lines now dedicated to the manufacture of products for two of our COVID-19 vaccine customers. We're also qualifying a high-speed syringe filling line at the site. This project was first announced in January 2019 and is expected to be operational in the next several months, in line with our original plan. Given the strong demand for biotherapeutic manufacturing, we will continue to invest in additional drug product and drug substance capacity at our Bloomington campus. Our 300,000 sq ft facility in Anagni, Italy, also continues to make significant contributions to the global supply of COVID-19 vaccines for multiple customers. The additional high-speed vial filling line we've accelerated for our vaccine customer is expected to be operational before the end of this calendar year. Last month, we announced a $100 million expansion project at our Anagni facility to add biologics drug substance manufacturing capabilities to the site, establishing our first drug substance capacity outside of the U.S. to support the growing European market demand for biologics manufacture and supply. The initial phase of the expansion includes installation of two 2,000-liter single-use bioreactors within new purpose-built manufacturing suites, associated investments to support clinical development, and investments to support late-stage and commercial tech transfers. This initial phase will also include the installation of all the needed infrastructure for further expansion in the future. The initial bioreactors are expected to be operational for customer projects late in fiscal 2023. Later phases of the planned expansion contemplate creating 16,000 liters of total flexible manufacturing capacity, enabling 2,000 liter to 8,000-liter batches. Also in Europe, we announced last summer further investments in a facility in Limoges, France, to create a European center of excellence for clinical Biologics formulation development and drug product fill finish services. These investments are on track to be completed by the end of fiscal 2022. The modernization of the 56,000 sq ft facility includes the installation of a high-speed flexible line capable of filling vials, syringes, or cartridges under isolator technology, as well as enhancements to its analytical and quality control laboratories. Our new center of excellence in Limoges will strengthen Catalent Biologics' global and European capacity and will also serve as a feeder for additional services at our Anagni and Brussels facilities. Moving to our cell and gene therapy offerings, we continue to add both capabilities and related capacity. We entered the cell therapy market in February 2020 and have rapidly built our infrastructure and capabilities. We recently completed the build-out of our GMP cell therapy suites in Houston, Texas, and have begun manufacturing for clinical supply. We're also progressing the build-out of our commercial-scale cell therapy manufacturing facility in Gosselies, which is on track to open in late fiscal 2022. We also continue to identify inorganic opportunities to grow our cell and gene therapy platform. Recently, we acquired RheinCell Therapeutics, a developer and manufacturer of GMP-grade human induced pluripotent stem cells or iPSCs. Importantly, iPSCs are an ethically sourced substitute for embryonic stem cells and have shown significant promise in regenerative medicine for a wide range of therapeutic indications. RheinCell expands our existing custom cell therapy process development and manufacturing capabilities with proprietary GMP cell lines for iPSC-based therapies and enables us to offer the building blocks to scale iPSC-based cell therapies while reducing the barriers cell therapy innovators would otherwise face to gain entry into the clinic. In February, we entered into the plasmid DNA market through the acquisition of Delphi Genetics, also located in Gosselies, now part of our European Cell Therapy Center of Excellence, together with the launch of plasmid DNA development and manufacturing capability through an organic investment at our Rockville, Maryland facility. We've since further expanded our European Cell Therapy Center of Excellence on our Gosselies campus with the acquisition of an additional 32,000 sq ft facility. This facility provides us with the capacity for commercial-scale plasmid DNA manufacturing up to 500-liter scale. With the integration of plasmid DNA into our overall cell and gene therapy offerings, choosing Catalent will allow customers to de-risk their supply chains and optimize their programs along the entire development pipeline. In gene therapy, viral vector manufacturing capacity continues to be in high demand with a growing number of gene therapy compounds currently in the industry's development pipeline, as well as for manufacturing viral-based COVID-19 vaccines. In fiscal 2021, we completed the build-out of commercial-scale manufacturing suites in the first building at our Maryland gene therapy campus. To meet the increasing demand we see, we're now outfitting the adjacent building to include at least 5 additional cGMP suites, a project that remains on track for completion by this time next year. Before reviewing the Bettera acquisition, I'd like to highlight our expanding corporate responsibility and ESG commitments and the additional progress we've made since our last update. As a leader in the growing CDMO industry, we understand the need to demonstrate our shared commitment sense of urgency, and value in contributing to the long-term sustainability of the entire biopharma sector. In June, I shared our long-term sustainability plans at the Biopharma CEO Investor Forum, and I encourage you to watch the presentation on our IR website. Since then, we formalized a commitment to the Science Based Targets initiative, joining a growing list of companies setting actionable science-based greenhouse gas emission reduction targets to limit global warming. This commitment includes calculating and reducing direct and indirect emissions, even as the company continues to evolve and grow. One of our first actions after making this commitment was to ensure that the energy we purchase for all our sites in North America, South America, and Europe, as well as the majority of our sites in Asia, is coming from renewable resources. As a result of our actions, 97% of all our electricity usage across the enterprise is now procured from renewable energy sources such as wind, solar, hydro, and biomass, an achievement that will contribute to our overall greenhouse gas reduction efforts. We will incorporate our work on Science Based Targets into our annual ESG report for fiscal 2021, which we expect to publish in the first quarter of calendar 2022. While I'm very proud of the items I just mentioned, and the many other items that have become part of Catalent's ESG progress over the last several years, there's still more work to do. For example, some of our top ESG goals for fiscal 2022 include continuing to improve employee diversity at all levels of the organization and meeting our commitment to be landfill-free by the end of fiscal 2024. Now on to slide nine. We're pleased to announce our agreement to acquire Bettera Wellness. We've been seeking the right opportunity to expand our participation in the nutraceuticals and nutritional supplements markets for quite some time, leveraging the accelerated growth dynamics of the space. Bettera is a leading developer and manufacturer of consumer-preferred gummies, soft chews, and lozenges for nutraceutical, functional, and botanical extract products. They have four state-of-the-art production facilities in the U.S. There is no question that Bettera is one of the leading independent suppliers in this high-growth, capacity-constrained portion of the market. Within the space, Bettera is well-known for its ability to partner with its customers to develop and manufacture a variety of high-quality delivery formats with differentiated flavors and superior consumer experience. It's clear to us that the specialized expertise of the team we'll be bringing on is unparalleled, and Bettera's customer relationships reflect that. The acquisition will enable Catalent, and specifically our Softgel and Oral Technologies, or SOT, segment, to expand our substantial existing consumer health platform with the fastest-growing wellness product offerings in this area and also expand our ready-to-market product library, as well as provide a variety of packaging options to meet customer needs. We're excited to have this opportunity to strengthen our partnerships with our customers across gummies, soft chews, and lozenges going forward. As part of today's announcement, we are also increasing our expectations for our long-term revenue growth rate for our SOT segment from 3%-5%, to 6%-8%, given the strength of our advanced offerings and product libraries and supported by the significant growth contributions that we expect from Bettera. Moving to the transaction details. We've agreed to acquire Bettera for $1 billion on a debt-free, cash-free basis, and we expect to close the transaction within the first half of this fiscal year. To date, the company generates approximately $150 million in sales at attractive margins, reflecting its premium offerings, and is growing at over 20% annually. We expect similar growth over the next several years. We plan to fund the acquisition with a combination of cash on hand, a partial drawdown of our revolving credit facility, and potentially the issuance of new debt, with a resulting net leverage ratio of approximately 3.1x at close. Like in some of our other recent acquisitions, we expect significant deleveraging in the near to medium term following closing and expect to maintain ample firepower for further strategic M&A. From an earnings perspective, we expect the acquisition to be accretive to ANI per share in the first year after close and significantly accretive thereafter. At Catalent, we pride ourselves on our ability to bring in new talent and capabilities, and we're looking forward to seamlessly integrating Bettera and welcoming its team of approximately 500 experienced and knowledgeable employees and formulators to Catalent. On the integration front, we've developed a detailed plan to support and accelerate Bettera's in-flight growth plans and have already identified work streams and leaders for integration. Let me now share some additional capability information and market trends as covered on slide 11. As I mentioned, we've been seeking the right entry point into the nutraceutical gummies, soft chews, and lozenges markets for some time. Importantly, Bettera is one of the few at-scale independent manufacturers in the market today and is a market leader across all three categories. In addition to Bettera's end-to-end solutions from development to commercial manufacturing and packaging, Bettera has an extensive library of ready-to-market formulations to accelerate product launches for partner brands. Importantly, Bettera has the ability to produce gummy formulations with both gelatin and plant-based technologies with kosher, halal, organic, and other certifications. Bettera also produces soft chews and, in particular, soft chews using the cold process, which is ideal for protecting heat-sensitive ingredients. Our consumer health customers are constantly asking Catalent for new formats in addition to our product library, and specifically ask about gummies and other engaging formats for their nutritional supplement and nutraceutical product concepts. We view Bettera as an innovation engine for emerging high-growth brands, and we're excited to begin working with our customers in this area going forward. One of the reasons we're focused on investing in these areas is that we believe Bettera is at the intersection of macro consumer health trends, with innovative delivery systems growing at roughly four times the pace of the traditional market. I would also note that about 2/3 of this capacity-constrained market is outsourced today. While the market for traditional delivery systems remains large, the innovative segment's recent explosive growth has increased its portion of the nutraceuticals market to close to $17 billion today, measured at the retail level, more than doubling its market size over the last five years. We expect Bettera to grow in excess of the innovative market as a whole in the near to medium future. Finally, on this subject, I want to emphasize at Catalent, we always have room to add leading high-growth premium CDMO franchises to our business. Bettera is the latest example in our tradition of high growth and earnings accretive strategic M&A, and we're excited to begin working with Bettera's employees and customers. I'll conclude my opening comments by saying that Catalent prides itself on a track record of successfully identifying, acquiring, and integrating world-class businesses with leading manufacturing and development capabilities. Over the last several years, we've transformed our portfolio, expanding capacity and capabilities across our service offerings. We're proud of the work we've accomplished. Our future has never looked brighter. As I look across our entire portfolio, I note again that we remain on track to meet or beat our goal of achieving 50% of our 2024 net revenue from our Biologics segment. We continue to forecast long-term growth in that segment in the range of 10%-15%. Based on our confidence in the growth we foresee across all of our segments, we're raising our projected consolidated long-term net revenue growth rate to 8%-10% from the previous 6%-8%, which we expect will be coupled with continued EBITDA margin expansion. We're confident in our trajectory and believe our announcement today is a testament to how our employees and partners have helped Catalent position itself for continued long-term growth. I'm now very happy to welcome Tom Castellano back to our earnings calls. As you know, Tom previously served as the company's investor relations officer through 2019 and was promoted on June 1st to CFO from his most recent role as global Vice President of operational finance. Welcome back, Tom Thanks, John. I'll begin this morning with a discussion on segment performance, where commentary around segment growth will be in constant currency. I'll start on slide 13 with Biologics, our largest business segment, which represented 48% of our net revenue in fiscal 2021, compared to 33% in fiscal 2020, and half of our net revenue in the fourth quarter, compared to 38% in the fourth quarter of last year. Biologics net revenue in Q4 of $603 million increased 66% compared to the fourth quarter of 2020, with segment EBITDA increasing 112% over the same period. All net revenue growth was essentially driven organically, and EBITDA growth was slightly impacted by 1% due to costs associated with scaling and integrating the cell therapy and plasmid DNA acquisitions we closed in fiscal 2021. The robust organic growth in our Biologics segment in the quarter was again driven by high demand across segment offerings, including drug product, drug substance, and viral vector manufacturing, along with bioanalytical services. The increase was primarily driven by COVID-19-related projects, which continued to contribute to both development and commercial revenue growth. The segment's EBITDA margin increased significantly year-on-year to just under 31%, compared to 24.3% in Q4 of last year, which is primarily attributable to increased capacity utilization and higher volumes manufactured. In fiscal 2022, we expect the Biologics segment will continue to grow net revenue at a double-digit pace, though not near the 88% growth rate the segment recorded in fiscal 2021. Please turn to slide 14, which represents results from our Softgel and Oral Technologies segment. Softgel and Oral Technologies net revenue of $301 million decreased 1% compared to the fourth quarter of 2020, with segment EBITDA increasing 6% over the same period. This slight decline in the net revenue continued to be driven by reduced volume demand for certain prescription products, as well as lower demand for consumer health products, particularly for cough, cold, and over-the-counter pain relief products. However, over the last couple of months, we have seen business begin to recover and expect a return to growth in fiscal 2022 as contemplated in our guidance. EBITDA margin and SOT grew 220 basis points over the fourth quarter of 2020 due to an increase in productivity and favorable product mix. Slide 15 shows the results of our Oral & Specialty Delivery segment, which were again impacted by the voluntary recall of a single product in our respiratory platform in September 2020 that we have previously discussed. As previously reviewed, this product had notably strong sales in Q4 of last year following its February 2020 launch, and also included a product participation component, creating difficult comparisons over the periods. There was an additional $3 million in recall-related costs recorded in the fourth quarter, bringing the total to $32 million for the fiscal year. With that background, the OSD segment recorded net revenue of $186 million in the quarter, which was down 19% compared to the fourth quarter of fiscal 2020. Segment EBITDA was $63 million, a 29% decline over the fourth quarter of 2020. When factoring out the net impact from the divestiture of our Blow-Fill-Seal business and the acquisition of Acorda Therapeutics' spray drying facility in February, organic revenue declined 4% and segment EBITDA declined 11%. Further, if you back out the revenue from the recalled product in the fourth quarter of fiscal 2020, the OSD segment would have shown mid-teens revenue growth this quarter, driven by growth in both commercial and development revenue. The OSD segment's fourth quarter results reflect continued momentum in our Zydis proprietary platform, which grew nicely despite some lingering consumer health pandemic-related headwinds. Each quarter, we disclose our long-cycle development revenue in the current year in order to provide additional insight into our long-cycle segment, which includes Biologics, Softgel and Oral Technologies $38 million, which is 51% above the development revenue recorded in the fourth quarter of fiscal 2020. Development revenue, which includes net revenue from certain COVID-19 related products approved for emergency use, represented 45% of our revenue in the fourth quarter compared period in the prior year. The strong growth in our Biologics business, including growth from the manufacture of COVID-19 vaccines and therapies approved for emergency use, was the biggest driver of the year-on-year changes. In the fourth quarter, our development pipeline led to 47 new product introductions, for a total of 139 in fiscal 2020. As shown on slide 16, our net revenue of $105 million over Q4 of 2020. This notable increase, while appropriately reflecting the many positive aspects at work in the segment, should also be understood in the context of the segment's decreased performance in the fourth quarter of fiscal 2020 when the global lockdowns and clinical trial disruptions due to the pandemic. Segment EBITDA was $31 million by strong demand in our manufacturing and packaging and storage and distribution offerings. Segment EBITDA margin was 29% over the fourth quarter of last year. As of June 30th, 2021, backlog for the CSS segment was $501 million at the end of last quarter, and up 18%. The segment recorded net new business wins of $119 million during the fourth quarter, a 14% of the prior year. The segment's trailing 12-month book-to-bill ratio is 1.3x. slide, adjusted EBITDA on slide 17. Our fourth quarter adjusted EBITDA increased 30% to $348 million in the fourth quarter of fiscal 2020. On a constant currency basis, our fourth quarter adjusted EBITDA increased 27% compared to the fourth quarter of fiscal 2020. As shown on slide 18, fourth quarter adjusted net income was $2.00 per diluted share, compared to adjusted net income of $154 million, or $0.90 per diluted share in the fourth quarter a year ago. Slide 19 shows our debt-related ratios and our capital. Our net leverage was 2.2x at June 30th compared to 2.3x at March 31st. We expect the acquisition of Bettera to increase ratio of 3x because we will fund the acquisition through deploying $57 million cash on hand and other liquid assets we are reporting as available as of June 30th under our revolving credit facility and potentially naturally delever from there, providing us with organic and inorganic growth. As just noted, our cash and cash equivalents balance at June 30th stood at $896 million, and our marketable securities were $71 million, giving us liquid assets of $967 million compared to cash and cash equivalents of $953 million and no marketable security as of June 30th, 2020. Moving on, our capital accelerate our organic growth plans. We expect our level of capital expenditures to remain elevated as a percentage of net revenue in fiscal 2022, when we expect that CapEx will be approximately 15%-16% of 2022 net revenue. Free cash flow in fiscal 2021 was negative $253 million, despite the higher level of EBITDA generated in the last year. This was due to our increase in capital spending and the cost of pandemic-related precautions, such as increased inventory levels and other supply chain mitigation efforts, as well as higher net receivables. In fiscal 2022, we expect to return to positive free cash flow as a result of our strong CapEx investments. As a final note on the balance sheet, I want to call out a disclosure in our 10-K annual report we filed. As of June 30th, we had one large customer that represented 15% of our net trade receivables. Usually, high concentration reflected a single point in time at the end of the fiscal year. I note that the customer significantly reduced this balance in the days following the quarter close, and the balance is now well below the 10% reporting threshold. Now, we turn to our financial outlook for fiscal 2022 as outlined on slide 20, which does not reflect the just-announced and still pending acquisition of Bettera. We expect $4.3 billion-$4.5 billion, representing growth of 8%-13% compared to fiscal 2021. FX is currently expected to have a minimal impact on our revenue growth as the declining euro is offset against the increase in British pound. We project that revenue from preexisting M&A activity will negatively impact our growth rate by 1 to 2 percentage points as the divestiture of the BFS business more than offset the multiple smaller acquisitions completed in fiscal 2021. We project organic revenue growth in each of our segments to be within or above the long-term growth range we have previously disclosed for each segment, leading to revenue growth at or above our new long-term revenue growth range of 8%-10%. For full-year adjusted EBITDA, we expect a range of $1.13 billion-$1.2 billion, representing growth of 11%-18% compared to fiscal 2021. Our business, where revenue and EBITDA generation is more weighted to the back half of the fiscal year. We expect full-year adjusted net income to $585 million-$650 million, representing growth of 7%-18% compared to fiscal 2021. We also expect our fully diluted share count on a weighted average basis for fiscal 2022 to be in the range of 181 million-183 million shares. This projection counts our Series A convertible preferred shares as if all were converted to common shares in accordance with their terms. We expect our consolidated and 25% for fiscal 2022. Now I'd like to close with a few comments regarding the revenue contribution from our array of COVID-19 response products. First, all of that revenue is considered organic revenue. Second, we now expect, particularly in light of the need to produce vaccine booster shots and address the growth in variant forms, that this revenue will have a multiyear duration. Third, as John said in his opening comments, our net COVID-related revenue in fiscal 2021 totaled more than $550 million. While we do not plan to disclose a forecast for growth related to COVID revenue in fiscal 2022, given the capacity we have dedicated to COVID-19 projects that was brought online in the last 9 months, we do expect continued growth from our work related to COVID-19 projects. In addition, we now see innovative vaccines, particularly the newer gene-based vaccines, as a long-term strategic product area for Catalent, given the substantial partnerships we have built in this space through the pandemic. Operator, this concludes our prepared remarks. We would now like to open the call for questions. As a reminder, to ask a question, please press star, then the number one on your telephone keypad. Again, that is star, then the number one. Your first question comes from Tycho Peterson with JP Morgan. Hey, good morning. I'll start with one on Bettera. It looks like this is basically 100% over-the-counter. Is that correct? Can you maybe just talk about how much of this was just about broadening the portfolio or is there a chance you could leverage some of the technology? This is clearly in the nutraceutical and nutrition category, there are no prescription products in there. Just as a reminder, you know this well, Tycho, that Catalent Health, we've always had important franchises. If you go into any CVS or Walgreens and just peruse the aisles, as well as many other products that people don't know are being manufactured by Catalent. This is 20% and 30% of our overall Softgel business and has been absolutely terrific. We've been looking to get into this area, honestly, for the last four to five years. We recognized it as an incredibly high-growth area We believe, given the know-how and expertise we have from an overall gelatin standpoint, we thought that we might be able to do this organically. The truth of the matter is, there's significant know-how and capabilities somewhat different from what we do in Soft that necessitated us to go and actually acquire one of the leading businesses in this overall area. What we also love about it is that given the strong relationships that we have with leading consumer healthcare companies that we're already partnered with from a VMS standpoint, that we're going to be able to leverage those relationships. The last thing I will tell you, Cook Pharmica, just like we did with Paragon, just like we're doing in MaSTherCell in the cell therapy area. Catalent is an operating company that does things to scale. We acquire assets and given the fact that this is a capacity-constrained area, we really believe that we can grow this business into the leading manufacturer of this unique delivery platform. Honestly, the margins are incredibly attractive. Great. That's helpful. On the near-term, obviously, you're not providing any guidance around COVID. I'm just curious, though. The White House is actually talking about an aggressive booster rollout plan starting next month. Is that kind of baked into the near-term outlook? Do you think the COVID tailwinds could be higher or in line or below, what you saw in 2021? Longer term, you're not really kind of quantifying the EBITDA margin expansion. Previously, you talked about 8%-11%. I'm just curious if you could give us any kind of directional color there. Thanks. Yeah, sure. First of all, it's becoming increasingly clear that COVID vaccines and also boosters are going to be part of the way forward here. Literally, when we're sitting with only 15% of the population of the world vaccinated and the variants coming out we see as we've noted in our prepared remarks that vaccines are really going to become part of actually the core Catalent business. I will tell you that all of the current contracts and to the vaccines are contemplated in our current guidance. Obviously there are situations a lot that just depends upon what actually happens there. All of the current information is currently baked into our overall guidance. I'll turn it over, Tom, for the back half of your question. Yeah, agree with everything John said there related to guidance. I would also add, Tycho, you're right. We didn't specifically highlight long-term EBITDA growth rates but did speak to the continued margin expansion we expect to see. As you remember, we mentioned working towards a 28% EBITDA margin for the business by 2024. We continue to believe that's a good target and are on pace for that, in growth with the 8%-10% revenue outlook we put out there. Okay. That's helpful. One last one before I hop off. Gene, you highlighted a lot of the capacity expansion in the RheinCell deal as well. I'm just curious, as you look at your portfolio economics capacity reservation fees, given a lot of the capacity that's going to be coming online, do you think that model still holds? First of all, I would just say that the dynamics continue to be extremely robust. I think over the last two years, we've really added critical pieces to our portfolio in the cell therapy space getting additional manufacturing facilities and capacity. We entered into the plasmid DNA space and now obviously with the acquisition of RheinCell. We really think but I will tell you that we have a very strong science and technology looking and continue to understand where the technology's going and where Catalent can take technology and capabilities. I would say that broadly speaking in the Biologics area, it's going to continue to take a large part of our overall growth CapEx for the company because we continue to see extremely strong pipelines. In this business as we've seen over and over again, if you have the right capacity at the right time. Gene therapy business is moving much in terms of making product to make even reservation fees that component of the early part of the business when we were literally dealing with a handful of suites within Catalent. It'll be somewhat part of the model, but it will not be the main part of the model. The bottom line is when we have capacity, customers want, we're able to actually bake the right deal in terms of what we would call site preparedness, equipment preparedness. If a customer has long-term forecasts and wants suites from us and we're absolutely going to go ahead and get reservation fees. I would say that was much more of a model in the early days, and now we're moving towards a model of just making literally hundreds of batches in our gene therapy business. Now a lot of the money is flowing from purely the work that we're doing. This is pure reservation fees. Okay, very helpful. Thank you. Your next question is from Jacob Johnson with Stephens. Hey, thanks. Congrats on the quarter. Maybe just a similar question what Peg just asked, but asked in a different way. The Bettera deal is a fairly significant deal to bolster the SOT segment after a variety of deals on the Biologics side. Is this a signal that you have the majority of the Biologics capabilities you need at this point, so we should think about the investments being largely organic on that side of the business in the near term? Well, clearly, I would say we're always on the hunt for great Biologics assets, period. With the platform that we have basically built through acquisition, we really believe we have a footprint where organic investment is going to continue to fuel our growth. In today's earnings prepared remarks, we talk about several significant expansions, whether it's in Anagni, whether it's in Limoges. I will say there are significant CapEx projects going on all across Catalent, and obviously, we're going to be seeing a high level of CapEx spend again this year. Catalent really does continue to be very active in the M&A market. We do feel that we have really the right set of assets on the Biologics front. Quite frankly, by being able to pivot here with really an exciting acquisition that's going to bolster our SOT business segment from 3% to 5% to 6% to 8%, and incredibly attractive margins in a capacity-constrained environment where this is what Catalent does. We operate at scale. Catalent's ability to scale up that business and drive to be number one in this innovative delivery platform is really what we have our sights set on. What I really do like about Catalent is it's a well-balanced business. Quite frankly, we've really been taxing pretty aggressively through the pandemic and the vaccines, our Biologics and gene therapy segment. Now this allows us in our SOT segment and to some extent our other segments to be able to use our leadership to build out a part of the business that's always been core, a critical platform has paid the bills with cash flow for many, many years. Again, absolutely a terrific acquisition for us, and we're excited to have the Bettera team as part of Catalent with their expertise and know-how. Jacob, I would only add to this one just around the margin profile John said in his prepared remarks as well as here around the attractiveness of the margins for Bettera. They're actually accretive, not only to the SOT segment, but to Catalent overall. Very strong financial profile here of the acquired business. Got it. Good. Got it. Thanks for that, John and Tom. Then maybe just the follow-up on that. John, you mentioned Anagni. You're adding drug substance capabilities there. You have both substance and product capabilities. Can you just talk about the synergies between having both those capabilities in a single campus? Yeah. No, it's a very big deal. Thank you for pointing out Anagni. First of all, I just want to say thanks to the Anagni leadership team. What they have done over the last 18 months has been absolutely phenomenal. Here in the U.S., we talk a lot about our Bloomington site, the Anagni site has literally been a marquee site for the European COVID-19 vaccine efforts. The team has really delivered flawlessly, literally more than 100 million vaccine doses that have come out of there. Just a terrific leadership team. I can tell you that the synergy between drug substance and drug product is huge. Actually, we have an offering for it within Catalent. It's called OneBio. Our ability to basically do cell line engineering, do drug substance scale-up into phase I, and then be able to put that into a finished drug dosage form format for clinical trials, and then ultimately scale up for manufacturing is absolutely huge. There are relatively few non-CDMOs that have that capability. Our biopharma customers, the large ones do. From a CDMO standpoint, I think Catalent is really up there with only maybe one other CDMO that is able to have drug substance or drug product. Even better if you can have it all in one campus, which is what we'll be able to do at Anagni. We've kind of announced the 2 by 2,000 L, but we're going to have the ability, obviously, to scale that up much more significantly. I think you're going to see Catalent become an extremely strong player from a biologics drug substance and drug product standpoint. Back to the previous question with regards to M&A and biologics. This is an area where although we have some terrific assets between our Brussels facility, our Limoges facility, our Anagni facility, where we're investing from a drug product and now also a drug substance standpoint. If we could secure additional drug substance and drug product assets in Europe, that would clearly be high on our priority list. We have been participating in quite a few processes, but haven't been able to land that one yet. We're clearly being aggressive on the overall organic front. Back to the question, the synergies between drug substance, drug product, and the OneBio offering we have, which is bringing in more and more customers, specifically the small- to medium-sized customers who want to have one-stop shopping from this standpoint is very significant. Got it. Thanks for taking the question. Thank you, Jacob. Your next question is from John Kreger with William Blair. John. Hey. A couple of CapEx questions. John, you mentioned Bettera and that whole space is capacity constrained. How is the available capacity in that asset that you're getting? Are you going to have to dedicate a fair amount of CapEx to keep up with the growth? Yeah. First of all, Bettera really is in a massive growth phase. As we've stated, they're growing at 20%. They have several in-flight CapEx investments. I'm sure at some point we'll be talking on these calls about something called a mogul, which is really the workhorse for the gummies area. We will be investing additional CapEx to scale that business. I will tell you that the CapEx levels of spend will be much lower than anything that we see from an overall Biologics standpoint, lower than what we see from an overall Catalent standpoint. Will probably be slightly higher, but more in line with what we've traditionally spent in our SOT segment, really making it, again, a strong cash generator at extremely attractive margins for the company. Great. Also, John, I think you told us that CapEx in the coming year should be 15%-16% of revenue. Should we start to think about that as sort of the new normal for the company longer? Look, we have to step back and remember that COVID was a massive accelerator for Catalent from a strategic standpoint. It actually accelerated our strategic plans, we brought on capacity earlier than we normally would have. That capacity post let's say largest volumes of vaccines in three, maybe four years is going to be reapplied to the overall company. I think we're seeing here over the first couple of years, obviously this accelerated CapEx spend. As we've kind of modeled out in our strategic plans, we see our CapEx spend moving much more towards that higher single digits CapEx spend that we had prior to going into overall COVID. I think that's the right way to look at the overall business. That being said, what we traditionally see is again, Catalent is a company that buys high growth assets and then scales them up. I will repeat, we are going to be looking to be the number one provider in the gummy categories over time. We take assets and we invest in them to make them leading franchises. If we were to not acquire anything else, I would see our CapEx moving down to that high single-digit level. Again, as we acquire assets, we do invest in them. It'll really be dependent upon what assets we get, John, whether or not we'll stay a slightly elevated area. Again, we love these projects because the IRR and cash on cash returns for the investments we're doing on the growth side, specifically in Biologics gene therapy and now in the gummy area, is going to be pretty fantastic. Sounds good. Thank you. Your next question is from Dave Windley with Jefferies. Hi. Thanks for taking my questions. John, I appreciated the emphasis you put on that answer to John. CapEx intensity will come down. Good to know. I'm wondering on the longer-term growth algo, I'm thinking about your biologics and COVID revenue within biologics and the handoff of that over the long term. Yeah. Is the extension of a booster market, does that make that much easier to manage that it's not going to be so sudden, but rather a longer, more protracted handoff to other products in the long term? Sure. First of all, we do not see a COVID cliff in Catalent. We recently came out of our strategic plans, and we modeled out, and this was in April. A lot of things have happened since then, but we modeled out three different scenarios. Right now, I would tell you that our current modeling against expected case is actually higher given the fact that we see vaccines for COVID specifically being really much more of a sustaining and an enduring revenue for Catalent, specifically with the advent of boosters that'll come out lowering the age of those vaccines, plus the large part of the world that still needs to get vaccinated. We're also seeing a change in formats where we want fewer doses per vial. We're seeing a push towards going towards prefilled syringe. Actually, all those things actually lend to increasing volumes for Catalent as you move towards either single dose or lower volume formats and also boosters. The other thing that I would tell you, Dave, is that Catalent has now put itself into the vaccine category in a really substantial way. It was always, I would say, a significant category within Catalent. It's now moved up within our overall look at the overall categories within Catalent, and with the capacity and capabilities, and quite frankly, the strong brand reputation of being able to deliver in this crazy tumultuous time of COVID vaccines has elevated our status as a CDMO in the vaccine category. We also see that mRNA is not just going to be a COVID vaccine therapeutic platform. As you know, Moderna had quite a large pipeline, if you will, of mRNA vaccines. We're partnered very closely with them with COVID. We certainly expect them as well as our other partner, J&J, to be using our expertise for non-COVID related vaccine items, which I won't detail here in the call. From a Catalent standpoint, again, COVID was an accelerator of our strategic plans. Quite frankly, our growth and our ability to upgrade our long-term guidance now from 6%-8%, to 8%-10% revenue growth, I think is a testament of that, and also points to the fact that, as you know, we've held onto our long-term growth guidance for quite some time, since 2014, before bringing it up with the acquisition of Paragon and now bringing it up here in this earnings call. That alone should tell you what our outlook is with regards to the growth rate of the company and how we see vaccines continuing to play a strong role into the future without any, I would say, substantial cliff in terms of the business since we'll be dovetailing in some of our strong pipeline along with the continued sustained supply required for the COVID vaccine. Sorry for the somewhat belabored answer, but it's a really important question, and it's important for me to be able to pass along all of that information broadly to the analysts and investors. Yeah. Thanks for the context there. I appreciate that. Quickly on margin. Margins were strong. Perhaps the composition of those was a little bit different than I and others expected. In the Biologics segment, could you comment on whether there was a mix change there, or you mentioned reservation fees in the context of another answer. Was there some impact that caused the Biologics margin to drop a little bit from what we've seen in the last couple of quarters? Yeah, Dave, Tom here. Just under 31% EBITDA margin for the fourth quarter here for the business. A great performance from where we were a year ago. You're right, sequentially is down from where we were at third quarter levels. I'd just point to a couple of things here. We have to remember that this is still primarily development business, and with that does come some, I would say, volume-related lumpiness that can have a negative impact on margins. The fact that we're seeing the sustainable margins within this business north of 30% is something right in line with where management expected it to be. The other thing I would highlight here is component sourcing continues to be a growing revenue stream within the business. These are the pass-through revenues associated with some of the components used for the vaccines. That comes in at a very low margin profile. We're seeing that increase having a little bit of a drag. The other thing I would say is, when we think about the level of maturity within our Cell & Gene Therapy business, Cell Therapy primarily, the investments that we continue to put into that business are relatively substantial from an operating cost perspective and do have a little bit of a headwind to the margin profile of Biologics. Again, I just want to highlight the 31% that we saw in the fourth quarter. Again, right in line with where we expected that to be from a management standpoint and seeing sustainable margins above 30% within Biologics. Got it. Thank you. Your next question is from Paul Knight with KeyBanc Capital Markets. Mike on for Paul. First one, John, it's nice to see Catalent continue to build out its presence in Biologics in Europe with the Anagni announcement. Just as a follow-up, you're obviously building out significant capacity in the U.S. related to viral vectors. Given the capacity constraint in that market, when does it start to make sense to have a presence there for viral vectors given your significant cell therapy and plasmid DNA presence already there? Actually, thank you for that highlight. I probably should have also noted that that is also a category that we are looking at within Europe. Clearly, we have got a strong footprint for cell therapy across our Gosselies, Belgium campus now and also Houston. We have a huge capability in viral vector manufacturing in the Baltimore area. If we were able to get our hands on the right asset from a viral vector manufacturing standpoint in Europe, that would also be a priority for us. We continue to see an extremely strong pipeline in the overall gene and cell therapy space, and I do believe that having assets in the right area are going to be key. We love being in Baltimore, given that that really is kind of a center from an overall, I would just say, virology standpoint. Clearly Europe will also be an area where we're going to continue to look for an asset there. If we're not able to get our hands on one, we may pursue the organic build-out route, but that would obviously take some additional time. Thank you for actually highlighting that. Just following up on Tom's past comment with respect to gene-based vaccines, specifically mRNA kind of having a long duration for Catalent outside of COVID. These type of vaccines and therapeutics are more challenging to deliver to the body. You have purchased the upstream tech with Delphi and historically been strong in fill and finish with therapeutics and vaccines. Obviously, you have the viral-based delivery technology with Paragon. Do other delivery technologies like lipid nanoparticles and electroporation kind of make sense for an R&D perspective or potential M&A perspective for Catalent? Thank you. Yeah. Certainly I would just say that LNP or lipid nanoparticles are a big part of the secret sauce for mRNA delivery. We know with regards to one very large specific provider that they've kept a lot of that in-house, and then with another provider, they are partnered, but there's a lot of wraps around, I would say, the know-how and the intellectual property of those LNPs. It is an area that is high on our list. I've actually had some dialogues with one large customer about the ability for Catalent to be their LNP provider, and based on the mRNA standpoint. We're early on in those discussions, but it is a key area. I have to emphasize again, I mentioned our science and technology team is constantly on the hunt for, and looking out with advanced radar to understand what are the key technologies and the key growth areas that Catalent needs to be participating in. An example of that is the RheinCell acquisition, which again, we think is going to be key for us in the cell therapy and regenerative medicine area. You'll continue to see Catalent bringing in those type of technologies into the company. Certainly, the mRNA space is going to continue to be, with two approved products here, it's clearly now it's going to be a therapeutic category where we're all going to be watching what they're going to be able to do beyond the vaccines. The great news is, we are partnered with clearly one of the best, if not the best in this area. Great. Thank you for the time. Your next question is from Sean Dodge with RBC Capital. Thanks. Good morning. Maybe going back to Bettera. On the margin, John, you said incredibly attractive already, accretive to the consolidated total. Is there any more specificity you can share there? Then just to better understand the trajectory or potential, I guess if we roll forward a few years of 20%+ revenue growth, is there a lot of opportunity to continue scaling those higher? Or with the tight capacity constraints, are things there as good as they could or should be, it's just more adding revenue at those margins? First let me just make the statement that this is a category that has biologics or higher margins to it. When we talk about it being accretive and then accretive to Catalent, that should give you your signal. Let me just back up a little bit here. Gummies have become the dominant experiential delivery format in VMS, and the VMS retail market is growing 3+ faster than the rate of over-the-counter. It's actually now larger than over-the-counter. Through the pandemic and even running up to the pandemic, wellness has really become something of a personal responsibility, and people are really going after nutritional, nutraceutical, and other functional areas. Gummies have been the format, in fact, launching the most number of products in this category compared to everybody else. Gummies have grown more than 20% year per year for the last four years and now represents more than 40 billion doses. The VMS segment is growing in mid-single digits, but gummies, despite representing less than 20% of delivery formats, have accounted for greater than 50% of total VMS growth over the last several years. Nearly 70% is outsourced with a limited number of CDMOs, and it's capacity constrained. Again, what does Catalent do well? We do things at scale. Our ability to scale this business appropriately to be able to not only grow with the market, but to grow substantially faster than the market that is capacity constrained compared to competition, is really where we're going to be able to drive this to be the number one franchise out there from a CDMO standpoint. That's why we got into this. It's really, again, a terrific business for us, very high margins, and one that Catalent can get its hands on, integrate, we have very detailed plans, and scale. Okay. Maybe scale is a little bit of the answer to my next question, but it's easy to see how Catalent can differentiate itself and sustain high margins in Biologics and cell and gene therapy, just given the scientific rigor involved there. On the Bettera side, maybe just could you talk a little bit more about what are the differentiating factors in the gummy or the nutraceutical market? What does the competitive moat look like there? To give you a sense for the level of difficulty, with all the capabilities that we have within Catalent, specifically in soft gel, gelatin, and the franchise that we've had there in the VMS standpoint, we were unable to attack this space organically. The reason is there's incredible amount of know-how in terms of developing these products with the right texture and flavors. This is not something that you can just buy a machine and go. It's really built upon the capability of the team to formulate those products. The other part of this is it's not just the ability to formulate, but proactively formulate these products because essentially what customers are buying are off-the-shelf products that have been already proactively developed. For Catalent, with all of our skills and capabilities, we really ran into a wall in terms of being able to build this business organically over the last five years and ultimately went down the inorganic front, found one of the leading players. We believe they're the number two player in the space, and our goal is to make them the number one player, pure and simple. Again, very substantial. I know that some people that don't understand Catalent very well will look at all of the Biologics, gene therapy, and cell therapy acquisitions that we've done and say, "I don't get it." That's because they don't understand the fact that we are supplying to biopharmaceutical customers and Consumer Health customers, and our Consumer Health customers have been a stable base for this company for many, many years. In fact, the team that had been here for 20+ years said that Catalent literally developed through our soft gel business, the cough and cold categories that we now see ubiquitously on the shelves of Walgreens, Walmart, and CVS. This is in our DNA. It requires innovation. There's a different clock speed that's required in this category, and we have longstanding relationships with all the big six players in the consumer health category, which again, the VMS category has been growing faster, 3x faster, than OTC. For Catalent, this actually was a natural, if not slightly late, acquisition into this very fast-growing space. Okay. That's great. Very helpful. Thanks again. Your next question is from Juan Avendano with Bank of America. Hello. Thank you. Just one question from me. You alluded to the change in the COVID vaccine packaging configuration in a previous answer. Can you tell us how is the potential revenue and margin from a fewer-dose format compare to the current format? By when would you anticipate this change to come to effect? I'll answer this at a high level that says that from a Catalent perspective, we are not paid per dose, we are paid per fill. If you have fills that are at a lower number of doses, it means you generally need more fills. From an overall Catalent perspective, it's a positive tailwind as you go to formats that have fewer doses per vial or potentially into the pre-fill syringe format, and you can expect those to be again at strong margins. Thank you. Your next question is from George Hill with Deutsche Bank. Hey, good morning, guys. Thanks for taking the question. I'm going to come back to the topic of M&A one last time, John and Tom, and maybe just talk about, John, you used pretty aggressive language earlier as it related to the company's M&A profile. I guess, can you talk about the processes that you went through that the company wasn't able to get to the goal line on? What was the barrier there? Was it valuation? Was it bidding environment? Was it not the right asset? You guys have been so successful. I'd like to hear more about what went wrong in the M&A process. I'm sorry. I didn't quite get the question about what went wrong on the M&A process. Can you just back up a little bit and re-explain? Yeah, sure. You talked about two bidding processes where you guys couldn't get to the goal line, and you guys have been very successful in M&A. I guess I'd like to hear more about what went wrong when you guys couldn't get deals through. What has been the barrier? Yeah, nothing went wrong. It's usually a case of us being disciplined acquirers, both in terms of valuation. I would say nothing's gone wrong in our process. At some point, the valuations get to a point where they didn't make sense from an overall Catalent perspective. I would just say that our processes are incredibly strong. They've led to the string of acquisitions that we've done, starting with Cook Pharmica, through Paragon, through MaSTherCell, through all of the campus that we built out in Gosselies. Again, doing M&A requires a certain level of discipline so that at some point the value for the asset doesn't make sense and we move on. Just put this under the category of disciplined acquirer where we moved on, and as you've seen, we've taken a path that doesn't limit us by expanding pretty quickly organically in the BMS facility that we purchased that's in Anagni as well as expanding our Limoges facility. We'll continue to aggressively look for those assets. M&A is not a purely deterministic activity, and it involves a lot of considerations in terms of moving forward in the process. That's what I expected. I appreciate it. Thanks, John. There are no further questions at this time. I will now hand the call back over to Mr. [John Chiminski, CEO], for final comments. Actually, John Chiminski will conclude here. Thanks, operator, thanks everyone for your questions and for taking the time to join our call. I'd like to close by highlighting a few key points we covered today. Fiscal 2021 was an incredible year for Catalent. We didn't just outperform our expectations for 2021 during a global crisis, but our rapid response to the pandemic gave us the opportunity to do real good for the entire world, provided an insightful demonstration of the depth of our capabilities, significantly elevated our brand, helped increase our engagement with our employees as we banded together to meet the challenges of the pandemic, and enabled us to accelerate our strategic plans and investments. In Fiscal 2022, we expect strong revenue and EBITDA growth again, driven by continued growth in our Biologics segment, as well as a return to growth in our SOT and OSD segments. Because of the investments we've made over the past few years, which included adding high-growth franchises like those we've acquired in our Biologics segment and like the one we now anticipate with Bettera, we're stronger and better positioned for long-term growth than ever before, as evidenced by the increase in our projected long-term net revenue growth target to 8%-10%. Finally, I'm very proud of the team of more than 17,000 and the way we've lived up to our mission to help people live better, healthier lives. When we look back at our last fiscal year, we know that across the 1,400 development programs we advanced and the 7,000 products we manufactured on behalf of our clients, we helped enhance the lives of millions of patients around the world. Thank you. Ladies and gentlemen, this concludes today's conference call. Thank you for participating. You may now disconnect.