Pharmaceutical & Biotech Contract Management Software
Secure, compliant document workflows for Life Sciences
Accelerate research, clinical trials, and regulatory processes with eSignatures and document automation built for compliance.
Join 68,000+ companies accelerating docs with PandaDoc
Why PandaDoc for Life Sciences?
Managing documents in the life sciences industry means balancing speed, collaboration, and strict compliance requirements. PandaDoc helps teams streamline contracts, clinical documentation, SOPs, and regulatory submissions — all while meeting industry standards like FDA 21 CFR Part 11.
Accelerate approvals
Reduce bottlenecks in research, clinical trials, and regulatory workflows.
Ensure compliance
Confidently meet FDA and international eSignature requirements.
Streamline collaboration
Enable cross-functional teams, CROs, and external partners to securely review and sign documents.
Maintain data integrity
Keep a verifiable, auditable record of every signature event.
Built-in security & compliance
PandaDoc provides the controls and safeguards you need to confidently manage electronic records and signatures
21 CFR Part 11–Compliant Workspaces
Ensure FDA-compliant electronic signatures and audit-ready records with enhanced signer verification, secure audit trails, and controlled user access.
eIDAS & Qualified Electronic Signatures (QES)
Expand compliance globally with EU-recognized standards.
Single Sign-On (SSO) & Advanced Authentication
Protect sensitive data and simplify secure access across your organization.
Tamper-Evident Audit Trails
Maintain transparency and integrity with detailed document history.
Customer stories
Thousands, 50,000 actually, use PandaDoc each day to make their document process painlessly simple.
Learn more about industry-specific PandaDoc offerings
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