Accelerate research, clinical trials, and regulatory processes with eSignatures and document automation built for compliance.
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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.
Reduce bottlenecks in research, clinical trials, and regulatory workflows.
Confidently meet FDA and international eSignature requirements.
Enable cross-functional teams, CROs, and external partners to securely review and sign documents.
Keep a verifiable, auditable record of every signature event.
PandaDoc provides the controls and safeguards you need to confidently manage electronic records and signatures
Ensure FDA-compliant electronic signatures and audit-ready records with enhanced signer verification, secure audit trails, and controlled user access.
Expand compliance globally with EU-recognized standards.
Protect sensitive data and simplify secure access across your organization.
Maintain transparency and integrity with detailed document history.
Thousands, 50,000 actually, use PandaDoc each day to make their document process painlessly simple.
Accelerate contract review, increase compliance, and streamline documentation
Streamline inventory control, sales, and operations
Improve your process, streamline business development, and empower your customers
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