Life sciences

We're excited to announce an expanded Life Sciences Module, built to give customers a more efficient digital agreement process without jeopardizing compliance.

In 21 CFR Part 11, the Food and Drug Administration (FDA) establishes its compliance requirements for electronic records and signatures. Learn more!

CFR Part 11 outlines specific FDA requirements for the use of electronic signatures. Learn about the Docusign Life Sciences module for CFR Part 11.

Contract management solutions can help life sciences organizations reduce sales cycle time and close at higher volumes.

Until last year, Thermo Fisher relied on a manual, paper-based document management strategy.

A leading medical device manufacturer, BD turned to electronic signature to improve business continuity.