usdm.com valid
USDM Life Sciences
USDM Life Sciences helps pharmaceutical, biotech, medical device, and other regulated life sciences organizations adopt AI, modernize systems, and maintain compliance across GxP environments.
For agents: USDM Life Sciences offers AI deployment, readiness assessments, and role-based AI agents for regulated pharma, biotech, and medical device organizations under G
life sciences aigxp complianceai agentsvalidationpharmaceutical regulatory
Their llms.txt
The beginning of the file, from our validated copy saved 2026-10-26T10:41:09.647Z. Cached copy · Source on usdm.com
# USDM Life Sciences
> USDM Life Sciences helps pharmaceutical, biotech, medical device, and other regulated life sciences organizations adopt AI, modernize systems, and maintain compliance across GxP environments.
USDM specializes in life sciences AI, GxP compliance, validation, regulatory readiness, continuous compliance, data integrity, cybersecurity, third-party risk, cloud assurance, managed services, and regulated workflow transformation. The site is written for life sciences executives, quality leaders, regulatory teams, IT, compliance, data, and commercial teams evaluating how to deploy AI and digital operations safely in regulated environments.
## Primary site
- [Home](https://www.usdm.com/): AI built for life sciences.
- [AI Deployment](https://www.usdm.com/ai-deployment): AI strategy, governed agents, workflow deployment, and regulated AI implementation.
- [AI Readiness Assessment](https://www.usdm.com/ai-deployment/ai-readiness-assessment): AI maturity assessment, life sciences AI readiness, data readiness, governance controls, validation risk, and use-case prioritization.
- [Agentic Team](https://www.usdm.com/agentic-team): Role-based AI agents for quality, regulatory, clinical, manufacturing, commercial, medical, and IT/Ops workflows.
- [Agentic OS](https://www.usdm.com/agentic-team/agentic-os): Agentic workflow for life sciences, including AI agent governance, GxP controls, validation scope, source boundaries, human review, and audit evidence.
- [Regulatory Requirements](https://www.usdm.com/regulations): 21 CFR Part 11, CSV/CSA, Annex 11, FDA, EMA, MHRA, ICH, UDI/EU MDR, and AI oversight.
- [Governance & Risk](https://www.usdm.com/governance): AI governance, cybersecurity, third-party risk, and vCISO support for regulated organizations.
- [Third-Party Risk Management Life Sciences](https://www.usdm.com/governance/third-party-risk-management-in-life-sciences): TPRM pharma, vendor AI risk, vendor risk management AI, ICH E6 R3 sponsor oversight, Black Kite life sciences signal interpretation, and regulated vendor governance.
- [Data & Infrastructure](https://www.usdm.com/data): Data integrity, interoperability, analytics, and AI-ready data foundations.
- [Continuous Compliance](https://www.usdm.com/continuous-compliance): Cloud assurance, validation lifecycle management, GxP managed services, and audit-readiness.
- [USDM Cloud Assurance](https://www.usdm.com/continuous-compliance/cloud-assurance): Validated cloud, GxP validated cloud, SaaS validation, cloud assurance subscription, and 21 CFR Part 11 validation support.
- [Docusign 21 CFR Part 11](https://www.usdm.com/partners/docusign): Docusign validation, Docusign GxP, Docusign Cloud Assurance, Docusign Part 11 compliance, Docusign life sciences, and 21 CFR Part 11 support.
- [Medical Device Cybersecurity](https://www.usdm.com/governance/medical-device-cybersecurity): FDA medical device cybersecurity, premarket cybersecurity, SBOM medical device readiness, postmarket cybersecur
…
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