Schrödinger, Inc. is an international scientific software and biotechnology company that specializes in developing computational tools and software for drug discovery and materials science. Schrödinger's software is used by pharmaceutical companies, biotech, tech, chemicals, energy, aerospace firms, and academic researchers to simulate and model the behavior of molecules at the atomic level. This accelerates the design and develops new drugs and materials more efficiently, reducing the time and cost of bringing them to market.3 It was founded by Richard A. Friesner and William Andrew Goddard III.1 Its shares trade on Nasdaq under the symbol SDGR.1Wikipedia text CC BY-SA 4.0
Schrödinger, Inc. is an international scientific software and biotechnology company that specializes in developing computational tools and software for drug discovery and materials science.3
Financials
From the company’s reports to the SEC. Every number links to the filing it came from.
Revenue1011126$255.9M in 2025+199% since 2019Gross profit101311126$142.6M in 2025+190% since 2019Operating income101311126-$166.9M in 2025+331% since 2019Net income101311126-$103.3M in 2025+320% since 2019
Revenue141516$58.9M in Q2 FY2026+8% since Q2 FY2025Gross profit141516$32.4M in Q2 FY2026+24% since Q2 FY2025Operating income141516-$41.5M in Q2 FY2026−21% since Q2 FY2025Net income141516$6.0M in Q2 FY2026
Every line of the income statement as filed: the last 3 fiscal years, latest first.6
Period ending
2025-12-31
2024-12-31
2023-12-31
Total revenues
$255.9M
$207.5M
$216.7M
Total cost of revenues
$113.3M
$75.5M
$76.0M
Gross profit
$142.6M
$132.1M
$140.7M
Research and development
$173.1M
$201.8M
$181.8M
Sales and marketing
$41.0M
$39.9M
$37.2M
General and administrative
$95.4M
$99.7M
$99.1M
Total operating expenses
$309.5M
$341.4M
$318.1M
Loss from operations
-$166.9M
-$209.3M
-$177.4M
Gain on equity investments
$0
$0
$147.2M
Change in fair value of equity investments
$48.2M
$5.7M
$53.5M
Other income
$16.4M
$17.9M
$19.7M
Total other income
$64.6M
$23.6M
$220.4M
(Loss) income before income taxes
-$102.3M
-$185.7M
$42.9M
Income tax expense
$939.0K
$1.4M
$2.2M
Net (loss) income
-$103.3M
-$187.1M
$40.7M
Net (loss) income per share attributable to common and limited common stockholders, basic (in USD per share)
-$1.41
-$2.57
$0.57
Weighted average shares used to compute net (loss) income per share of common and limited common stockholders, basic (in shares)
73.4M shares
72.7M shares
71.8M shares
Net (loss) income per share of common and limited common stockholders, diluted (in USD per share)
-$1.41
-$2.57
$0.54
Weighted average shares used to compute net (loss) income per share of common and limited common stockholders, diluted (in shares)
73.4M shares
72.7M shares
75.0M shares
No quarter-by-quarter statement was filed.
Total assets17101311126$726.2M in 2025+368% since 2019Total liabilities17101311126$362.1M in 2025+535% since 2019Shareholders’ equity1017126$364.1M in 2025Cash10171311126$230.5M in 2025+197% since 2018
Total assets18151614$640.4M in Q2 FY2026−7% since Q2 FY2025Total liabilities18151614$311.4M in Q2 FY2026−10% since Q2 FY2025Shareholders’ equity141516$329.0M in Q2 FY2026−4% since Q2 FY2025Cash18151614$287.9M in Q2 FY2026+31% since Q2 FY2025
Every line of the balance sheet as filed: the last 4 fiscal years (annual) or 4 quarters (quarterly), latest first.6
Period ending
2025-12-31
2024-12-31
2023-12-31
2022-12-31
Cash and cash equivalents
$230.5M
$147.3M
Restricted cash
$6.9M
$15.3M
Marketable securities
$164.9M
$204.8M
Accounts receivable, net of allowance for doubtful accounts of $440 and $210
$83.0M
$235.7M
Unbilled and other receivables, net of allowance for unbilled receivables of $140 and $100
$21.4M
$19.6M
Prepaid expenses
$12.5M
$12.2M
Total current assets
$519.3M
$635.0M
Property and equipment, net
$19.5M
$24.2M
Equity investments
$73.6M
$43.2M
Goodwill
$4.8M
$4.8M
Right of use assets - operating leases
$102.7M
$111.9M
Other assets
$6.3M
$4.2M
Total assets
$726.2M
$823.2M
Accounts payable
$11.5M
$10.7M
Accrued payroll, taxes, and benefits
$39.3M
$42.1M
Deferred revenue
$112.9M
$111.9M
Lease liabilities - operating leases
$16.4M
$16.8M
Other accrued liabilities
$9.2M
$10.3M
Total current liabilities
$189.1M
$191.7M
Deferred revenue, long-term
$78.9M
$108.8M
Lease liabilities - operating leases, long-term
$92.8M
$101.1M
Other liabilities, long-term
$1.3M
$146.0K
Total liabilities
$362.1M
$401.8M
Preferred stock, $0.01 par value. Authorized 10,000,000 shares; zero shares issued and outstanding at December 31, 2025 and December 31, 2024, respectively
$0
$0
Additional paid-in capital
$992.0M
$946.0M
Accumulated deficit
-$628.8M
-$525.5M
Accumulated other comprehensive income
$107.0K
$220.0K
Total stockholders' equity
$364.1M
$421.4M
$548.6M
$447.9M
Total liabilities and stockholders' equity
$726.2M
$823.2M
Allowance for doubtful accounts receivable
$440.0K
$210.0K
Allowance for unbilled receivable
$140.0K
$100.0K
Preferred stock, par value (in USD per share)
$0.01
$0.01
Preferred stock, shares authorized (in shares)
10.0M shares
10.0M shares
Preferred stock, shares issued (in shares)
0 shares
0 shares
Preferred stock, shares outstanding (in shares)
0 shares
0 shares
Period ending
2025-12-31
2024-12-31
2023-12-31
2022-12-31
Cash and cash equivalents
$230.5M
$147.3M
Restricted cash
$6.9M
$15.3M
Marketable securities
$164.9M
$204.8M
Accounts receivable, net of allowance for doubtful accounts of $440 and $210
$83.0M
$235.7M
Unbilled and other receivables, net of allowance for unbilled receivables of $140 and $100
$21.4M
$19.6M
Prepaid expenses
$12.5M
$12.2M
Total current assets
$519.3M
$635.0M
Property and equipment, net
$19.5M
$24.2M
Equity investments
$73.6M
$43.2M
Goodwill
$4.8M
$4.8M
Right of use assets - operating leases
$102.7M
$111.9M
Other assets
$6.3M
$4.2M
Total assets
$726.2M
$823.2M
Accounts payable
$11.5M
$10.7M
Accrued payroll, taxes, and benefits
$39.3M
$42.1M
Deferred revenue
$112.9M
$111.9M
Lease liabilities - operating leases
$16.4M
$16.8M
Other accrued liabilities
$9.2M
$10.3M
Total current liabilities
$189.1M
$191.7M
Deferred revenue, long-term
$78.9M
$108.8M
Lease liabilities - operating leases, long-term
$92.8M
$101.1M
Other liabilities, long-term
$1.3M
$146.0K
Total liabilities
$362.1M
$401.8M
Preferred stock, $0.01 par value. Authorized 10,000,000 shares; zero shares issued and outstanding at December 31, 2025 and December 31, 2024, respectively
$0
$0
Additional paid-in capital
$992.0M
$946.0M
Accumulated deficit
-$628.8M
-$525.5M
Accumulated other comprehensive income
$107.0K
$220.0K
Total stockholders' equity
$364.1M
$421.4M
$548.6M
$447.9M
Total liabilities and stockholders' equity
$726.2M
$823.2M
Allowance for doubtful accounts receivable
$440.0K
$210.0K
Allowance for unbilled receivable
$140.0K
$100.0K
Preferred stock, par value (in USD per share)
$0.01
$0.01
Preferred stock, shares authorized (in shares)
10.0M shares
10.0M shares
Preferred stock, shares issued (in shares)
0 shares
0 shares
Preferred stock, shares outstanding (in shares)
0 shares
0 shares
Cash from operations101311126$13.9M in 2025Capital spending101311126$1.4M in 2025−21% since 2019Free cash flow101311126$12.5M in 2025
Cash flow is reported year to date, not quarter by quarter, so there are no separate quarterly figures.
Every line of the cash flow as filed: the last 3 fiscal years, latest first.6
Period ending
2025-12-31
2024-12-31
2023-12-31
Net (loss) income
-$103.3M
-$187.1M
$40.7M
Gain on equity investments
$0
$0
-$147.2M
Changes in fair value of equity investments
-$48.2M
-$5.7M
-$53.5M
Depreciation and amortization
$6.0M
$6.2M
$5.6M
Stock-based compensation
$43.0M
$49.9M
$47.8M
Noncash investment accretion
-$1.9M
-$7.6M
-$7.8M
Loss on disposal of property and equipment
$20.0K
$8.0K
$142.0K
Accounts receivable, net
$152.7M
-$169.7M
-$10.0M
Unbilled and other receivables
-$1.7M
$3.5M
-$10.0M
Reduction in the carrying amount of right of use assets - operating leases
$9.1M
$8.9M
$7.8M
Prepaid expenses and other assets
-$2.4M
-$3.5M
-$8.5M
Accounts payable
$908.0K
-$6.1M
$7.3M
Accrued payroll, taxes, and benefits
-$2.8M
$10.3M
$6.9M
Deferred revenue
-$29.0M
$155.5M
-$18.3M
Lease liabilities - operating leases
-$8.6M
-$10.1M
-$3.7M
Other accrued liabilities
$91.0K
-$1.9M
$5.9M
Net cash provided by (used in) operating activities
$13.9M
-$157.4M
-$136.7M
Purchases of property and equipment
-$1.4M
-$7.3M
-$13.4M
Purchases of equity investments
$0
-$3.1M
-$4.1M
Distribution from equity investment
$0
$0
$147.2M
Proceeds from sale and disposition of equity investments
$17.7M
$48.8M
$0
Purchases of marketable securities
-$313.0M
-$251.3M
-$320.6M
Proceeds from maturity of marketable securities
$354.6M
$361.8M
$384.0M
Net cash provided by investing activities
$57.9M
$148.8M
$193.0M
Proceeds from issuances of common stock upon stock option exercises
$3.0M
$1.5M
$9.4M
Proceeds from issuance of common stock in ATM offering
$0
$8.9M
$0
Payment of offering costs
$0
-$177.0K
-$373.0K
Principal payments on finance leases
-$58.0K
-$58.0K
-$19.0K
Net cash provided by financing activities
$2.9M
$10.1M
$9.0M
Net increase in cash and cash equivalents and restricted cash
$74.7M
$1.6M
$65.3M
Purchases of property and equipment in accounts payable
$40.0K
$162.0K
$192.0K
Purchases of property and equipment in accrued liabilities
$81.0K
$157.0K
$457.0K
Acquisition of right of use assets - operating leases, contingency resolution
$0
$2.8M
$514.0K
Acquisition of right of use assets in exchange for lease liabilities - operating leases
$0
$0
$15.1M
Acquisition of right of use assets in exchange for lease liabilities - finance leases
Schrödinger sits at the top of its group. 5 entities, 5 countries on record. Switch between the flow chart and the network, and select any entity to see its details.
Major holders of Schrödinger
Rubric Capital Management LPFiled SCHEDULE 13G/A on Schrödinger, latest May 15, 2026 (4 filings since Nov 13, 2024)
Sumitomo Mitsui Trust GroupFiled SCHEDULE 13G/A on Schrödinger, latest Apr 30, 2026 (3 filings since Feb 4, 2025)
David E. ShawFiled SC 13G/A on Schrödinger, latest Dec 1, 2021
SchrödingerWilmington, Delaware, United States
Reo Discovery Limited Subsidiary · Ireland
Schrodinger Korea LLC Subsidiary · South Korea
Schrödinger India Private Limited Subsidiary · India
Schrödinger Technologies Ltd Subsidiary · United Kingdom
Built from parent and subsidiary links from GLEIF, the Global Legal Entity Identifier Foundation (CC0); subsidiaries listed in Exhibit 21 of annual reports filed with the SEC; major holders from Schedules 13D and 13G. Each entity in the chart links to its source.
What it owns
What Schrödinger reports owning in its annual reports to the SEC: buildings, land and equipment, real estate and locations, investments, intangible assets and inventory, at the end of its latest fiscal year and a year before.
Our principal facilities consist of office space. We occupy approximately 136,047 square feet of office space in New York, New York under a lease that currently expires in December 2037, 35,000 square feet of office space in Portland, Oregon under a lease that currently expires in September 2026, and 48,987 square feet of office space in Hyderabad, India under a lease that currently expires in April 2028. Additionally, we lease office space at our other office locations around the world. We believe our facilities are adequate and suitable for our current needs and that should it be needed, suitable additional or alternative space will be available to accommodate our operations.
Schrödinger's computational platforms evaluate compounds in silico, with experimental accuracy on properties such as binding affinity and solubility. The company's products include molecular modeling programs in life science, and Materials Science, and an Enterprise Informatics Platform named LiveDesign, which is intended to facilitate communication among interdisciplinary research teams.
Small Molecular Discovery
Structure Prediction & Target Enablement
Hit Discovery
Hit-to-Lead & Lead Optimization
Read the full text
Drug Formulation
Biologics Discovery
Antibody Design
Peptide Discovery
Enzyme Engineering
Material Science Applications
Organic Electronics
Polymeric Materials
Consumer Packaged Goods
Catalysis & Reactivity
Thin Film Processing Energy Capture & Storage
Pharmaceutical Formulations & Delivery
Metals, Alloys & Ceramics
In addition to computational platforms, Schrödinger develops custom software for enterprises, as well as training, computer-cluster design and implementation, and research-based drug discovery projects.
Schrödinger software licenses are available to academic institutions for education and not-for-profit research.
Feb 26, 2025Reported quarterly or annual results63
Nov 12, 2024Reported quarterly or annual results64
Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). The full markets calendar
Filings
288 filings to the SEC since October 2021: 5 annual reports, 15 quarterly reports, 44 major events, 135 insider forms, 21 large holders, 68 other. The latest 20:
45 open-market trades by officers, directors and large owners since October 2021: 0 buys and 45 sales. Grants, option exercises and gifts are left out.
What the company paid its top executives, from the summary compensation table in its proxy statement. Total pay includes salary, bonus, stock and option awards and other pay, as the company valued them.
The largest holders among investment managers' 13F reports for the quarter ending Jun 30, 2026, the top 25 of 100. Change is in shares since the quarter before.
From the cover page of the 10-K filed Feb 25, 2026 (Section 12(b) of the Exchange Act).19
Risk factors and legal proceedings
The risks Schrödinger names in Item 1A of its 10-K filed Feb 25, 2026: 73 risks under these headings, as written.19
Risks Related to Our Financial Position and Need for Additional Capital
We have a history of significant operating losses, and we expect to incur losses over the next several years.
If we are unable to increase sales of our software, increase revenue from our drug discovery collaborations, or if we and our current and future collaborators are unable to successfully develop and commercialize drug products, our revenues may be insufficient for us to achieve or maintain profitability.
Our quarterly and annual results may fluctuate significantly, which could adversely impact the value of our common stock.
We will likely require additional capital to fund our operations. If we are unable to raise additional capital on terms acceptable to us or at all or generate cash flows necessary to maintain or expand our operations, we may not be able to compete successfully, which would harm our business, operations, and financial condition.
Raising additional capital may cause dilution to our stockholders, restrict our operations, or require us to relinquish rights to our technologies or drug programs.
If our estimates, judgments or assumptions relating to our critical accounting policies prove to be incorrect or financial reporting standards or interpretations change, our results of operations could be adversely affected.
Risks Related to Our Software
If our existing customers do not renew their licenses, do not buy additional solutions from us, or renew at lower prices, our business and operating results will suffer.
Our software sales cycle can vary and be long and unpredictable.
A significant portion of our revenues are generated by sales to life sciences industry customers, and factors that adversely affect this industry could adversely affect our software sales.
The markets in which we participate are highly competitive, and if we do not compete effectively, our business and operating results could be adversely affected.
The other 63 risks
We have invested and expect to continue to invest in research and development efforts that further enhance our computational platform. Such investments may affect our operating results, and, if the return on these investments is lower or develops more slowly than we expect, our revenue and operating results may suffer.
If we are unable to collect receivables from our customers, our operating results may be adversely affected.
Defects or disruptions in our solutions could result in diminishing demand for our solutions, a reduction in our revenues, and subject us to substantial liability.
We rely upon third-party providers of cloud-based infrastructure to host our software solutions. Any disruption in the operations of these third-party providers, limitations on capacity, or interference with our use could adversely affect our business, financial condition, and results of operations.
If our security measures are breached or unauthorized access to customer data is otherwise obtained, our solutions may be perceived as not being secure, customers may reduce the use of or stop using our solutions, and we may incur significant liabilities.
Any failure to offer high-quality technical support services could adversely affect our relationships with our customers and our operating results.
Our solutions utilize third-party open-source software, and any failure to comply with the terms of one or more of these open-source software licenses could adversely affect our business or our ability to sell our software solutions, subject us to litigation, or create potential liability.
Risks Related to Drug Discovery
We may never realize a return on our investment of resources and cash in our drug discovery collaborations.
We may not realize returns on our equity investments in our drug discovery collaborators.
Our drug discovery collaborators have significant discretion in determining when to make announcements, if any, about the status of our collaborations, including about clinical developments and timelines for advancing collaborative programs, and the price of our common stock may decline as a result of announcements of unexpected results or developments.
Although we believe that our computational platform has the potential to identify more promising molecules than traditional methods and to accelerate drug discovery, our focus on using our platform technology to discover and design molecules with therapeutic potential may not result in the discovery and development of commercially viable products for us or our collaborators.
We may not be successful in our efforts to identify, discover or develop product candidates and may fail to capitalize on programs, collaborations, or product candidates that may present a greater commercial opportunity or for which there is a greater likelihood of success.
We rely on contract research organizations to synthesize any molecules with therapeutic potential that we discover. If such organizations do not meet our supply requirements, or if such organizations do not otherwise perform satisfactorily, development of any product candidate we may develop may be delayed.
If we are not able to establish or maintain collaborations to develop and commercialize any of the product candidates we discover internally, we may have to alter our development and commercialization plans for those product candidates and our business could be adversely affected.
As a company, we have very limited experience in clinical development, which may adversely impact the likelihood that we will be successful in advancing our programs.
Conducting successful clinical trials requires the enrollment of a sufficient number of patients, and suitable patients may be difficult to identify and recruit.
We rely on, and plan to continue to rely on, third parties to conduct our clinical trials, and those third parties may not perform satisfactorily, including failing to meet deadlines for the completion of such trials, which may prevent or delay our ability to seek or obtain marketing approval for or commercialize our product candidates or otherwise harm our business.
Our reliance on third parties to manufacture our product candidates increases the risk that we will not have sufficient quantities of our product candidates or products or such quantities at an acceptable cost, which could delay, prevent or impair our development or commercialization efforts.
If serious adverse or unacceptable side effects are identified during the development or commercialization of our product candidates, we may need to abandon or limit our development and/or commercialization efforts for such product candidates.
The outcome of preclinical studies and early clinical trials may not be predictive of the success of later clinical trials, and the results of our clinical trials may not satisfy the requirements of the FDA or other comparable foreign regulatory authorities.
Interim, initial, "topline", and preliminary data from our clinical trials that we announce or publish in the future may change as more patient data become available and are subject to audit and verification procedures that could result in material changes in the final data.
We conduct, and we intend to continue to conduct, clinical trials for our product candidates at sites outside the United States. The FDA may not accept data from trials conducted in such locations, and the conduct of trials outside the United States could subject us to additional delays and expense.
If we and any current or future collaborators are unable to successfully complete clinical development, obtain regulatory approval for, or commercialize any product candidates, or experience delays in doing so, our business may be materially harmed.
Even if any product candidate that we may develop receives marketing approval, it may fail to achieve the degree of market acceptance by physicians, patients, third-party payers and others in the medical community necessary for commercial success.
Clinical trial and product liability lawsuits against us could divert our resources, could cause us to incur substantial liabilities and could limit commercialization of our product candidates.
We face substantial competition, which may result in others discovering, developing or commercializing products before or more successfully than we do, thus rendering our products non-competitive, obsolete or reducing the size of our market.
Risks Related to Our Operations
Doing business internationally creates operational and financial risks for our business.
If we fail to manage our technical operations infrastructure, our existing customers, and our internal drug discovery team, may experience service outages, and our new customers may experience delays in the deployment of our solutions.
Changes in tax laws or in their implementation or interpretation could adversely affect our business and financial condition.
Our ability to use our NOLs and research and development tax credit carryforwards to offset future taxable income may be subject to certain limitations.
Our international operations subject us to potentially adverse tax consequences.
Taxing authorities may successfully assert that we should have collected or in the future should collect sales and use, value added, or similar taxes, and we could be subject to tax liabilities with respect to past or future sales, which could adversely affect our results of operations.
Unanticipated changes in our effective tax rate could harm our future results.
We have acquired, and we may again in the future acquire, companies, businesses, solutions or technologies, which could divert our management’s attention, result in additional dilution to our stockholders, and otherwise disrupt our operations and adversely affect our operating results.
Our operations may be interrupted by the occurrence of a natural disaster or other catastrophic event at our primary facilities.
Risks Related to Our Intellectual Property
If we fail to comply with our obligations under our existing license agreements with Columbia University, under any of our other intellectual property licenses, or under any future intellectual property licenses, or otherwise experience disruptions to our business relationships with our current or any future licensors, we could lose intellectual property rights that are important to our business.
Our obligations under our existing or future drug discovery collaboration agreements may limit our intellectual property rights that are important to our business. Further, if we fail to comply with our obligations under our existing or future collaboration agreements, or otherwise experience disruptions to our business relationships with our prior, current, or future collaborators, we could lose intellectual property rights that are important to our business.
If we are unable to obtain, maintain, enforce, and protect patent protection for our technology and product candidates or if the scope of the patent protection obtained is not sufficiently broad, our competitors could develop and commercialize technology and products similar or identical to ours, and our ability to successfully develop and commercialize our technology and product candidates may be adversely affected.
Changes to patent laws in the United States and other jurisdictions could diminish the value of patents in general, thereby impairing our ability to protect our products.
Obtaining and maintaining our patent protection depends on compliance with various deadlines and procedural, document submission, fee payment and other requirements imposed by governmental patent agencies, and our patent protection could be reduced or eliminated if we fail to comply with these deadlines and requirements. We may miss a filing deadline for patent protection on these inventions.
Intellectual property rights do not guarantee commercial success of current or future product candidates or other business activities. Numerous factors may limit any potential competitive advantage provided by our intellectual property rights.
We, our prior, existing, or future collaborators, and our existing or future licensors, may become involved in lawsuits to protect or enforce our patent or other intellectual property rights, which could be expensive, time-consuming and unsuccessful.
Third parties may initiate legal proceedings alleging that we are infringing, misappropriating or otherwise violating their intellectual property rights, the outcome of which would be uncertain and could have a material adverse effect on the success of our business.
We may be subject to claims by third parties asserting that our employees, consultants, or contractors have wrongfully used or disclosed confidential information of third parties, or we have wrongfully used or disclosed alleged trade secrets of their current or former employers or claims asserting we have misappropriated their intellectual property, or claiming ownership of what we regard as our own intellectual property.
If we are unable to protect the confidentiality of our trade secrets, our business and competitive position may be harmed.
If our product candidates or any of our future product candidates obtain regulatory approval, additional competitors could enter the market with generic versions of such products, which may result in a material decline in sales of our competing products.
Risks Related to Regulatory and Other Legal Compliance Matters
Even if we complete the necessary preclinical studies and clinical trials, the regulatory approval process is expensive, time consuming and uncertain and may prevent us from obtaining approvals for the commercialization of some or all of our product candidates. As a result, we cannot predict when or if, and in which territories, we will obtain marketing approval to commercialize a product candidate.
Failure to obtain marketing approval in foreign jurisdictions would prevent any product candidates we may develop from being marketed in such jurisdictions, which, in turn, would materially impair our ability to generate revenue.
We have and may continue to seek certain designations for our product candidates, including Breakthrough Therapy, Fast Track and Priority Review designations in the United States, and PRIME Designation in the European Union, but we might not receive such designations, and even if we do, such designations may not lead to a faster development or regulatory review or approval process.
We may not be able to obtain orphan drug exclusivity for any product candidates we may develop, and even if we do, that exclusivity may not prevent the FDA or the EMA from approving other competing products.
Even if we, or any collaborators we may have, obtain marketing approvals for any product candidates we may develop, the terms of approvals and ongoing regulation of our products could require the substantial expenditure of resources and may limit how we, or they, manufacture and market such products, which could materially impair our ability to generate revenue.
Disruptions at the FDA and other government agencies from funding cuts, personnel losses, regulatory reform, government shutdowns and other developments could hinder our ability to obtain guidance from the FDA regarding our programs and develop and secure approval of our product candidates in a timely manner, which would negatively impact our business.
Current and future legislation may increase the difficulty and cost for us to obtain reimbursement for any of our product candidates that do receive marketing approval.
The prices of prescription pharmaceuticals in the United States and foreign jurisdictions are subject to considerable legislative and executive actions and could impact the prices we obtain for our products, if and when licensed, as well as impact our ability to find collaborators for our drug discovery programs on commercially acceptable terms.
Compliance with global privacy and data security requirements could result in additional costs and liabilities to us or inhibit our ability to collect and process data globally, and the failure to comply with such requirements could subject us to significant fines and penalties, which may have a material adverse effect on our business, financial condition, or results of operations.
We, and the collaborators who use our computational platform, may be subject to applicable anti-kickback, fraud and abuse, false claims, transparency, health information privacy and security, and other healthcare laws and regulations. Failure to comply with such laws and regulations, may result in substantial penalties.
We are subject to anti-corruption laws, as well as export control laws, customs laws, sanctions laws, and other laws governing our operations. If we fail to comply with these laws, we could be subject to civil or criminal penalties, other remedial measures, and legal expenses, be precluded from developing, manufacturing, and selling certain products outside the United States or be required to develop and implement costly compliance programs, which could adversely affect our business, results of operations and financial condition.
Changes in and uncertainty surrounding U.S. and international trade policies, particularly with respect to China, may adversely impact our business and operating results.
Our employees, independent contractors, consultants, and vendors may engage in misconduct or other improper activities, including non-compliance with regulatory standards and requirements and insider trading laws, which could cause significant liability for us and harm our reputation.
Our internal information technology systems, or those of our third-party vendors, contractors, or consultants, may fail or suffer security breaches, loss or leakage of data, and other disruptions, which could result in a material disruption of
our services, compromise sensitive information related to our business, or prevent us from accessing critical information, potentially exposing us to liability or otherwise adversely affecting our business.
Climate change-related risks and uncertainties and legal or regulatory responses to climate change could negatively impact our business, financial condition, results of operations, prospects and reputation.
Risks Related to Employee Matters and Managing Growth
Our future success depends on our ability to retain key executives and to attract, retain, and motivate qualified personnel.
Legal proceedings
From time to time, we may become involved in legal proceedings arising in the ordinary course of our business. We are not currently subject to any material legal proceedings.