Privacy & disclaimer

Privacy statement

• No account is required.
• This website and the Workspace set no cookies and use no browser storage (localStorage, sessionStorage or IndexedDB), no service workers, analytics, tracking pixels, heatmaps or session replay.
• Oncotics runs no backend, proxy, database or logging service for the Workspace. Session data lives only in your browser’s memory and is cleared on refresh or Clear Session.
• Requests are sent directly to public providers such as CIViC, ClinicalTrials.gov, openFDA, EMBL-EBI services, RxNorm and others. Each provider may log requests according to its own policy.
• Link-out sources open directly in your browser; some may be in languages other than English.
• Exports (JSON, CSV, print) are generated on your device and are never uploaded. File names never contain your search terms.
• An optional openFDA API key, if you enter one, is kept only in memory for the session. Keys used in a browser are not secrets.
• Your web host may keep standard server access logs for this website’s pages (for example IP address and page requested) for security and operations; Oncotics does not use them to profile visitors. Workspace searches are not sent to this server.

Do not enter personal health information

Do not enter patient identifiers, names, dates of birth, medical record numbers, raw genomic files (VCF, FASTQ, BAM), family medical records, device serial or implant lot numbers tied to a patient, or free-text clinical notes. The Workspace rejects inputs that look like this.

Medical, regulatory and procurement disclaimer

• This tool is provided for educational and research purposes only. Do not use it for direct patient treatment decisions without qualified clinical review.
• Trial information, FDA label and device data, genomic annotations, variant predictions, literature, pathway, interaction, target validation and cancer genomics data may change and may be incomplete.
• Computational predictions are not clinical diagnoses. Trial listings do not determine eligibility. Adverse event and MAUDE reports are voluntary and do not prove causality.
• Device clearance (510(k)/De Novo) is not approval (PMA/HDE/CDH). openFDA device data may lag the official FDA record; the official FDA database and your institution’s process are authoritative. Recalls require institutional action; Oncotics surfaces records only.
• Companion-diagnostic links are derived from label and device text and may be incomplete; the FDA companion-diagnostics list and current drug label are authoritative. LDTs are regulated differently from FDA-cleared or approved IVDs.
• Target validation signals are research evidence, not treatment recommendations.

Legal

• © 2026 Oncotics™. All rights reserved.
• Oncotics™ is a trademark of Oncotics.
• Oncotics™ does not provide medical, regulatory, or procurement advice and is not responsible for clinical decisions made using this interface.
• ClinicalTrials.gov data is provided by the U.S. National Library of Medicine. openFDA data is provided by the U.S. Food and Drug Administration. CIViC data is provided by the CIViC project. Ensembl, Europe PMC and other EMBL-EBI data are provided by EMBL-EBI. UniProt data is provided by the UniProt consortium. RxNorm data is provided by the National Library of Medicine. MyGene.info and MyVariant.info data are provided by their respective services.
• Oncotics™ is an independent interface and is not affiliated with or endorsed by these providers unless expressly stated.

Questions? Contact Oncotics.