Greetings, welcome to the Simulations Plus second quarter fiscal 2023 financial results conference call. At this time, all participants are in a listen-only mode. A brief question and answer session will follow the formal presentation. If anyone should require operator assistance during the conference, please press star zero on your telephone keypad. As a reminder, this conference is being recorded. It is now my pleasure to introduce Brian Siegel from Hayden IR. Thank you, Mr. Siegel. You may begin. Good afternoon, everyone. Welcome to our second quarter fiscal 2023 financial results conference call. With me today is our CEO, Shawn O'Connor, and our CFO, Will Frederick. After their portion of the call, we will open the floor to questions. Before we begin, I want to remind everyone that except for historical information, the matters discussed in this presentation are forward-looking statements that involve risks and uncertainties. Words like believe, expect, and anticipate refer to our best estimates as of this call, and there can be no assurances that these will actually take place. Our actual future results could differ significantly from these statements. Further information on the company's risk factors is contained in the company's quarterly and annual reports and filed with the US SEC. With that said, I would like to turn the call over to Shawn O'Connor. Shawn? Thank you, Brian. Thank you all for joining us on our second quarter conference call. This was a solid quarter for Simulations Plus. Second quarter revenue grew 6% year-over-year. Our software business grew 7%, generally in line with expectations reflecting the changes we proactively made in our renewal program, and the service business grew by 4% year-over-year, highlighted by the PK/PD and PBPK offerings. From a profitability perspective, we maintained solid margins and saw improvement over the first quarter as revenues grew, leading to $4.2 million of net income or $0.20 per diluted share. This result exceeded our guidance for the quarter. We continue to successfully navigate a challenging economy and its impact on our sales cycle. Drug developers are delaying purchases and elongating the sales cycle. For the most part, we have not lost opportunities, but this did impact our growth in the second quarter. I'd reiterate that we have taken this into account when preparing our 2023 full year outlook. Second quarter was highlighted by significant collaborative work with both partners and in support of our clients. To begin with, we have, in the last month, announced two collaborations involving our Artificial Intelligence machine learning technologies. Both the Institute of Medical Biology of the Polish Academy of Sciences and Sino-American Cancer Foundation partnerships will leverage our expertise in AI machine learning technologies to help with the discovery of novel molecules against two different emerging cancer targets. The computational and medicinal chemists in our early drug discovery services team will work with them to utilize the cutting edge AIDD technology in our ADMET Predictor software platform to accelerate the design and optimization of novel lead molecules. Our primary objective in these collaborations is to demonstrate the value of our AI machine learning technology and the capabilities of our drug discovery team in support of our software licensing and consulting service practice and in our market growth in these two areas. Both collaborations do provide for incremental benefits of joint compound ownership or milestone payments if successful. We're very excited about the opportunities these two collaborations represent. We entered into a new pKa collaboration with a large agrochemical company, extending machine learning models into a new and different space and broadening our addressable market. Our team will use the partner company's proprietary measurements drawn from its vast internal databases to build and refine a predictive model that can accurately predict the PK values of various chemical compounds. Additionally, we will create and evaluate new algorithms and techniques to further enhance the predictive capabilities of the model. We also submitted four FDA grant applications, one for ocular PBPK, another for lipid-based formulations, and finally, PBPK precision dosing and virtual BE workflows. Our relationship and collaborations with the FDA to extend modeling functionalities have always been a strength for Simulations Plus. A global biopharmaceutical company strategically partnered with us to apply GastroPlus PBPK modeling for their biosimilars project. Preclinical and clinical PBPK models are developed for the reference antibody injectable formulation and applied to predict bioequivalence for the prototype test formulations in development. The simulation results helped the company decide on the final formulation to advance into the pivotal study and minimize the risk of a failed outcome. Applications of GastroPlus in the biologics and biosimilars market is an emerging opportunity for us. A clinical stage precision medicine company outsourced GastroPlus PBPK modeling support to our experts for the lead and backup compounds with the simulation results informing their clinical candidate selection in the upcoming first in human study designs for their IND file. The confidence our partner obtained from these activities helped convince them to onboard the software for use internally across their entire pipeline. This quarter, Simulations Plus' service team provided pharmacometric modeling and simulation support for multiple high-profile regulatory submissions, including one compound offering novel treatment for a rare genetic disease, and two other compounds considered to be among the most anticipated drug launches in 2023. Finally, we expanded our growing opportunity as a consultant for investors, successfully selling our services for another even larger QSP project to provide insight to an investment group looking to invest in public-private companies. This follows the successful NAFLDsym project last quarter. Our ability to utilize public data and information to help investors make an informed decision is creating a new opportunity for us. These highlights demonstrate the numerous ways we assist our clients utilizing model-informed drug development approaches. Moving to our software business, revenues were up 7% in the quarter. As we have previously stated, we are taking deliberate actions with our software customers to align software renewal timing, which we expect to impact our first quarter revenue seasonality with our second through fourth quarter revenues being more evenly dispersed in absolute dollars. This trend line and new seasonality pattern was evident in the second fiscal quarter. We believe the renewal harmonization initiative is having the expected results of efficiency for ourselves and our customers and should be completed during the fiscal year. While quarterly software revenue growth rates are being impacted by this change in seasonality, we anticipate its impact on year-over-year software revenue growth to be minimal, and it's contemplated in our guidance. Our sales cycle is being impacted by economic concerns as sales to several potential new clients were pushed out, but not lost. We also had several smaller biotechs not renew due to cost containment measures implemented more dramatically in this market segment and the economic headwinds that are impacting funding for that part of the market. At the same time, we are achieving success in rolling out price increases reflective of our increased costs, which somewhat offset slower new sales cycles and contribute to higher gross margins and higher average revenue per account. GastroPlus was hit hardest in the first quarter by renewal alignment, but as expected, it rebounded nicely with 18% growth in the second quarter. We added 6 new customers, including business sourced in China. Of note, we brought a brand new distributor on in Brazil, which booked its first sale during the quarter. We also made 6 upsells to existing customers and saw 25 peer-reviewed published journal articles. These are all positive data points. MonolixSuite revenue declined 8% in the quarter, due mostly to the software harmonization process and foreign exchange impact. We added five new customers and made six upsells to existing customers during the quarter and feel good about returning to growth over the next few quarters. ADMET Predictor, which received the largest impact from the loss of the small biotech customers, saw revenue decline of 2% in the second quarter. Despite this, we added one new commercial customer and made eight upsells to existing customers in the quarter. Our University Plus program continued to grow and now represents 278 licenses in 54 countries. The program integrates our software into educational facilities and makes it part of advanced curricula, while feeding the market of next generation modeling and simulation professionals to drive future growth. Momentum in our services business continued in the second quarter with 4% revenue growth and backlog growth to $15.4 million. Operationally, we hired two consultants, adding to the five we hired in the first quarter. We believe these professionals will help convert backlog to revenue in the coming quarters. We performed 188 projects during the quarter. PKPD revenue increased 19% this quarter. We continue to experience a shift to higher margin time and material contracts from fixed price projects, which contributed to expanding our services gross margins. QSP/QST revenue decreased 32% for the quarter due to the more volatile nature of these high dollar value, excuse me, longer life cycle projects. As a reminder, in the second quarter last year, we had significant CRO passthrough revenue, creating a challenging comparison for this business. PBPK revenue increased 29% for the quarter, reflecting the deeper implementation of PBPK modeling, including an overall expansion of use cases and higher perceived value and impact. As we discussed last quarter, we evolved our capital allocation strategy, including the implementation of an accelerated share repurchase program, which began in January, and an ongoing cash dividend. As a reminder, we have three areas of focus. First, internal investment, which drives organic growth. Second is corporate development, which drives inorganic growth. Finally, returns capital to shareholders. With regard to return of capital to shareholders, the board approved a $50 million buyback program. Given our current cash position and Free Cash Flow, we believe we can still execute corporate development initiatives while offsetting a portion of the dilution from the 2020 capital raise. We initiated the share repurchase program with a $20 million ASR, which is currently being affected with an anticipated conclusion in the third quarter. Looking to the remainder of fiscal 2023, we maintain the guidance we provided at the beginning of our fiscal year. As a reminder, our full year revenue target is 10%-15% organic growth, which translates to $59.3 million-$62 million. As we said last quarter, we will continue investing in our people while selectively adding headcount in certain areas to support our long-term growth targets. This means fiscal 2023 will be a transition year for our cost structure, leading to lower margins and restraining EPS and EBITDA growth. We believe these actions are prudent and will benefit our long-term revenue growth while returning to a model with strong operating leverage. We expect to achieve diluted earnings per share of $0.63-$0.67, which translates to 5%-10% growth. Let me turn it to Will to discuss the financial results. Thank you, Shawn. Total revenue increased 6% for the quarter, comprised of 7% software growth and 4% services growth. Software represented 67% of revenue during the quarter. Total revenue increased 2% year-to-date, comprised of a 3% decrease in software revenue and 11% services growth. Software represented 60% of revenue during the year. Gross margin for the quarter improved year-over-year to 83%, reflecting the higher software mix and improved services margins. Software gross margin remained flat at 92%, and services margin increased to 66% compared to last year due to increased pricing and improved utilization. Gross margin year-to-date improved year-over-year to 81%, reflecting improved services margins. Software gross margin decreased slightly to 90%, and services margin increased to 68%. For the quarter, GastroPlus represented 55% of software revenue. MonolixSuite was 20%, ADMET Predictor was 18%, and other software was 7%. Year to date, GastroPlus represented 53% of software revenue. MonolixSuite was 22%, ADMET Predictor was 18%, and other software was 7%. For the quarter, our customer renewal rate was 94% based on fees and 80% based on accounts. These lower rates reflect the renewal timing changes Shawn mentioned, as well as the impact from smaller biotech customer non-renewals. Generally, the smaller customer non-renewals were offset with our price increases, as reflected in the higher fee-based renewal rates. The increase in average revenue per customer is reflective of the higher prices, combined with the loss of smaller biotech companies, as well as the seasonality of our software business. We expect quarterly comparisons to prior periods to fluctuate throughout the fiscal year with our new seasonal expectations. Year to date, our customer renewal rate was 93% based on fees and 81% based on accounts. Average revenue per customer increased to $103,000. Shifting to our services business. The services revenue breakdown for the quarter was 50% from PK/PD services, 20% from QSP/QST services, 23% from PBPK services, and 7% from other services. The services revenue breakdown year to date was 49% from PK/PD services, 19% from QSP/QST services, 24% from PBPK services, and 8% from other services. Other services consist primarily of regulatory services we provide our customers to help them meet global regulatory compliance and quality requirements. We also provide comprehensive learning services focused on modeling and simulation training with a variety of options to help our customers succeed. Total services projects worked on during the quarter decreased 6% compared to last year, and backlog decreased by approximately $2 million from last year to approximately $15 million. The decreases are primarily due to the QSP/QST services business. Turning to our consolidated income statement for the quarter. Total R&D costs were $2.1 million or 14% of revenue, compared to $1.6 million or 11% of revenue last year. R&D expenses were $1.3 million or 8% of revenue, compared to $0.9 million or 6% of revenue last year. Capitalized R&D was $0.8 million or 5% of revenue, compared to $0.7 million, also 5% of revenue last year. SG&A expense was $7.8 million or 49% of revenue, compared to $5.6 million or 38% of revenue last year. Scientific headcount and compensation increases were the most significant driver of this increase. Income from operations decreased 26% to $4 million, while operating margin was 26% compared to 37% last year. Interest in other income was $1 million this quarter versus $0.1 million last year. This reflects stronger returns from higher interest rates on our investment portfolio balance. Income tax expense was $0.9 million compared to $1.1 million last year, reflecting an effective tax rate of 18% this year compared to 20% last year. Net income decreased 5% to $4.2 million, and diluted earnings per share decreased to $0.20. The revenue impact for the quarter from foreign currency exchange was $0.2 million, and expenses related to M&A during the quarter were $0.1 million, for a total of $0.3 million or about $0.01 in diluted earnings per share. Adjusted EBITDA was $6.2 million, and adjusted EBITDA margin was 40% compared to adjusted EBITDA of $7.2 million or 48% margin last year. As a reminder, we calculate adjusted EBITDA by adding back stock-based compensation expenses and expenses related to M&A or other non-cash, non-operating expenses. We provide a reconciliation of this non-GAAP metric to net income, the relevant GAAP metric, in our earnings release and on our website. Turning to our consolidated income statement year to date, total R&D costs were $4.2 million or 15% of revenue, compared to $3.3 million or 12% of revenue last year. R&D expenses were $2.5 million or 9% of revenue, compared to $1.8 million or 7% of revenue last year. Capitalized R&D was $1.7 million or 6% of revenue, compared to $1.5 million, also 6% of revenue last year. SG&A expense was $15 million or 54% of revenue, compared to $10.6 million or 39% of revenue last year. Income from operations decreased 47% to $4.9 million, while operating margin was 18% compared to 34% last year. Interest and other income was $1.8 million versus $0.1 million last year. Income tax expense was $1.3 million compared to $2 million last year, reflecting an effective tax rate of 19% this year compared to 21% last year. We expect our effective tax rate for the fiscal year to be in the range of 19%-20%. Net income decreased 27% to $5.4 million and diluted earnings per share decreased to $0.26. The revenue impact year to date from foreign currency exchange was $0.5 million and expenses related to M&A during the year were $0.4 million for a total of $0.9 million or about $0.04 in diluted earnings per share. Adjusted EBITDA was $9.2 million and adjusted EBITDA margin was 33% compared to adjusted EBITDA of $12.4 million or 46% margin last year. We ended the quarter with cash and short-term investments of $115 million and no debt. During the quarter, we paid Morgan Stanley $20 million under our accelerated stock repurchase agreement and received an initial delivery of 408,685 shares of our common stock. These shares were retired and are treated as authorized unissued shares. The final number of shares to be repurchased will be based on the volume-weighted average price of our common stock during the term of the ASR agreement, less a discount and subject to adjustments. The final settlement is expected to be completed during the third quarter. We currently estimate the final share to delivery to be approximately 85,000-95,000 shares. We continue to be well capitalized and combined with our free cash flow, we believe we have sufficient resources to support our capital allocation initiatives and continued pursuit of strategic acquisitions and investments. I'll now turn the call back to you, Shawn. Thank you, Will. The quarter generally unfolded as we expected, and the adjustments to our renewal strategy are progressing well, putting us on track to achieve our full-year goals. Foreign exchange rates continue to create headwinds and the general economy is impacting our sales cycle, particularly for smaller biotech companies. We are navigating these challenges, driving profitable growth, generating cash and returning capital to shareholders. I'm proud that we continue to deliver on our commitment to science, driving greater adoption of in silico tools to accelerate innovation and reduce costs. We are investing in internal R&D efforts to maintain and grow our leadership position, and our increased scale enables us to expand our industry collaborations. We continue expanding our strong global regulatory relationships and now have multiple FDA technology development collaborations. In conclusion, we are confident in our ability to execute against our plan and achieve our guidance for fiscal 2023. Thank you for your time and attention. We will now turn the call over to the operator for the question and answer session. Thank you. Ladies and gentlemen, at this time we will be conducting a question and answer session. If you'd like to ask a question, you may press star one on your telephone keypad. A confirmation tone will indicate your line is in the question queue. You may press star two if you would like to remove your question from the queue. For participants using speaker equipment, it may be necessary to pick up your handset before pressing the star key. Our first question comes from the line of François Brisebois with Oppenheimer & Co. Please proceed with your question. Hi, thanks for taking the question. Just a first one from me is just, in terms of the revenue growth and the confidence and hitting the end of year guidance, can you just maybe help us, just clarify what metrics or maybe qualitatively what it is just based on the quarter here that keeps you confident in achieving that year-end revenue goal? Yeah, Frank, you know, the renewal harmonization program really, you know, has jumbled the renewal dates through the course of the year and impacting our quarter delivery of software revenue. The activity through the first couple of quarters in that regard has gone as anticipated, and still believe pretty strongly that the renewal rates will be complete. That harmonization process will be complete by the end of the year. On a year-over-year basis, we should see, you know, a normalized revenue growth in terms of the software business. That inevitably meant that with a seasonality pattern last year, low first and fourth quarter, and this year with a low first quarter, even lower first quarter, and a more comparable second, third and fourth quarter delivery of revenue. That the, you know, growth rates in terms of the first half of the years were gonna be depressed and the growth rates in the third quarter and especially the fourth quarter, where last year was a very low revenue quarter, would be exaggerated in the fourth quarter, evening out as we get to the end of the year. The, you know, qualitative indicators that were on that path are the harmonization program, slotting in, pretty much as anticipated, going into the year. Okay, great. Great. That extension and sales cycle that we expected, the new seasonality, it's not, you know, you wouldn't say this quarter kind of showed that look, it was a little bit worse than expected. It's still fairly in line and we're dealing with it. Yeah, no, it's fairly in line in terms of the harmonization program. Certainly, you know, we're seeing elongation of some sales cycles here, independent of the harmonization program as we see the, you know, macro economic environment slow down purchasing departments in our client industries, and especially in that segment in biotech. We're managing our way through that. On the other side, you know, a price increase that we put in place at the beginning of the year, before the beginning of the year is yielding a pretty good contribution to offset those economic challenges that we're running into. Number of variables coming into play, all of which come down and net out to a reconfirmation of our guidance as provided at the beginning of the year. Okay, great. Then on the side, you know, given the economic backdrop and what's been going on, you know, that part of the prepared remarks just discussing the new hires that you're making, these are very specialized hires. You know, can you maybe comment, is it only new hires or has there been, you know, a loss of personnel as well on the other side? If there is a loss, is it kind of normal rate of loss? Just trying to get a feel for whether or not there's more people net-net or pretty much the same kind of sales force, I guess, or consulting force? Primarily focused on the scientific consulting group. You know, it's a net plus for the organization year to date here through two quarters. Good recruiting, good hiring, success on that side and on retention. You know, very positive. I can't say that we haven't lost anyone, certainly compared to last year, the retention side is shored up. We invested quite a bit at the end of last year in terms of, you know, our review of, you know, all aspects of working for Simulations Plus, big component of which is compensation, but other factors, and implemented some programs that we thought would contribute to a tapering off in terms of any retention challenges that we had with the demand that was in the marketplace for skilled people that we have on board and support our recruiting efforts into fiscal year 2023. Quite pleased with the results of that investment to date. Okay, great. That's it for me. Thank you, and congrats on the progress. Yeah, take care, Frank. Our next question comes from the line of Matt Hewitt with Craig-Hallum. Please proceed with your question. Good afternoon. Thank you for taking the questions. Maybe first up regarding the synchronization process, it sounds like you're pretty much complete on the GastroPlus side. Sounds like you've got a little bit more work to do on the MonolixSuite side of the equation. Is that something you expect to wrap up here in the third quarter, or is that maybe a one or a two quarter process to complete that? Yeah, Matt, it's a, by the end of the year process. I wouldn't characterize that the process is done even for GastroPlus. While we did see that growth rate bounce back up to 18% in the second quarter. There is still a combination of movement on the renewal side there with that product that still has to play out. I think, you know, we're certainly halfway through it, if you will, halfway through the year, making progress, but there's still some hard work to do by the team. Okay. I think, Will, you provided a little bit of color on the renewal rates that dipped a little bit here in the second quarter. Is that pretty much a function of this synchronization process, or is there maybe something else? Does that speak to a little bit on the delays on signing new contracts that I think, you spoke to, Shawn? Yeah. It's a combination of some of the smaller biotechs that aren't renewing just with the environment out there for them to get financing. The rest of it's tied to the synchronization process and the timing for those renewals. Got it. Then regarding the new collaborations, obviously, congratulations on both of those. I'm just curious, how should we be thinking about the size of those potential milestones? Is there the potential for royalties, if those molecules are ultimately approved by regulatory agencies? Who will own the molecule? Any additional color on the, maybe the structure of the contracts would be helpful. Sure, sure. Yeah, very excited about the two partnerships that we've put in place. Want to emphasize that our focus here is in terms of demonstrating the value and capabilities of our AI machine learning technology, working with two organizations that will supply the, you know, the data, in many cases, the knowledge of the target, and the candidates. Our drug services support team will provide the support along with our technology to apply our AI/ML technology to the generation process there. Very hopeful that it produces success with a focus on it being a driver in terms of our software licensing business and our consulting business in this area. Having those case studies and success stories is what will drive that. As you know, our focus has been in terms of being a tool provider to our clients as opposed to a drug developer. Now, you enter into these relationships, and one of the benefits of them is that it's very common for some shared success triggers to be involved. In one case, it is joint ownership of compounds that may come out of the program. In the other case, it's a defined royalty stream associated with them. While that's not our primary focus, it is a nice icing on the cake opportunity. Understand that these programs do take some time to come to fruition. I don't see any impact from those two opportunities in the near term future for us. Certainly a nice opportunity in the long run. Well, that's great. Obviously, we'll hopefully you'll keep us apprised as those progress. Then, and maybe one last one, and I'm not sure if you're gonna have this handy, but I'll throw it out there anyway. You did mention you're basically moving into a couple new markets. I'm just curious, one being outside of therapeutics, it sounded like. Are there TAMs associated with those market opportunities, or were these more very early stage one-off situations if, depending upon how things go, then maybe it becomes a new market for you? Thank you. Yeah, Matt. The agrochemical partnership, that collaboration that we've been working there certainly opens up more business opportunity for our support in that industry segment, which we have a very small footprint in. Today, 5% of our business is done outside of the pharma world in support of cosmetics industry and other adjacencies. This would go into that bucket and certainly would add some TAM to our opportunity on a go-forward basis. The other one I think you might be referring to is the biologics collaboration. That certainly is not a brand new market for us. We do participate in that market already. Increasing our functionality footprint, and experience in that area gives us, more opportunity to take market share in that segment. Got it. All right. Thank you so much. Take care, Matt. Our next question comes from the line of Mitra Ramgopal with Sidoti & Company. Please proceed with your question. Yes, good afternoon. Thanks for taking the questions. First, just curious on the, on the churn, you were seeing on the small biotech accounts, if that's continuing now into the third quarter. Is it stabilizing or is it even moving on to maybe medium-sized companies? It continues into the third quarter. It's, it's evolving in terms of growing up scale. I mean, you know, large pharma and, you know, larger medium-sized biotech companies have experienced slowdown as well. It's not virgin territory in those other categories, but it's been more dramatic in the small biotech space where funding is a little bit more critical, near-term funding is critical. Smaller pipelines of candidates, so on and so forth. Certainly the challenges that they face continue into this quarter. I know at the market level, we're seeing some more activity in terms of potential funding, opening up of funding in the biotech space. Takes a while for that to trickle back down into the marketplace, cash in the hands of the small biotech and opening up of purchasing, you know, plans. You know, while macro there might be some positive signs, at on the ground level, it's still a battle for them. Okay, thanks. Just coming back to the recent hires, if that's included in the guidance in terms of expected contribution or is that more fiscal 2024? We've seen new hires come, you know, up and running and contributing billable time quite quickly in terms of our most recent experience. We won't be waiting for them to contribute until the next fiscal year. No, we're not not changing our guidance to raise it because of the success we've had on the recruiting side at this point. Okay. Thanks. Finally on inorganic opportunities. I know you've mentioned in the past you have a lot, you've been evaluating, but nothing has closed, so to speak. Just wondering your level of optimism given the current environment and your strong cash position, et cetera. If, we should be expecting something on that front over the next, 12 months. Yeah, you know, Mitra, it's hard to ever put any time constraints around those things. Certainly, it is a very active area for us. A number of discussions and efforts and investment in that space. I'm sure that we will find ourselves happily making an announcement at some point here down the road. Can't really put brackets around the timing of that. You know, that's great. Well, thanks again for taking the questions. Very good. Take care, Mitra. As a reminder, it is star one to ask a question. Our next question comes from the line of Dane Leone with Raymond James. Please proceed with your question. Pat, thanks very much. Two questions from me. One, could you just give us the estimate in terms of the expected EPS impact from the buyback this year? Secondly, are there any particular therapeutic verticals that you saw in the quarter that had more strength in terms of projects or, you know, were particularly weak, driving some of the drop in service revenue? Thank you. I'll go backwards in terms of the service revenue and the therapeutic areas. You know, no real change in the dynamic that we've seen as to spending on the oncology front, neuroscience front. Those areas are quite active across, you know, multiple therapeutic areas. You know, the service revenue drop this quarter really focused in terms of our QSP, QST consulting business, where that business with its sort of typical $1 million, sometimes $2 million projects that it performs can be relatively lumpy and, you know, not really therapeutic driven in terms of its cadence of projects. It's not really a therapeutic area challenge there. It's just the timing of the large projects. Last year we had a significant revenue quarter in the second quarter for that group. Their comparable was a bit of a challenge. Will, you wanna help out on the EPS side in terms of the impact of the stock buyback? Sure. With the ASR that we've got underway, you know, netted against the cash that we used and the interest we could earn, it's about a, I'll call it about a $0.01 improvement to EPS, which is included in our guidance. There are no further questions in the queue. I'd like to hand the call back to Shawn O'Connor for closing remarks. Very good. Well, I appreciate everyone's attention today and support of Simulations Plus. Look forward to speaking again in a few months with our third quarter results. Take care, everyone. Ladies and gentlemen, this does conclude today's teleconference. Thank you for your participation. You may disconnect your lines at this time. Have a wonderful day.