Configuring Acrobat Sign for Healthcare, Life Science & FDA-Regulated Best Practices
Navigating e-signature compliance in regulated environments — from FDA 21 CFR Part 11 to HIPAA — can feel overwhelming without the right configuration and support in place. Acrobat Sign includes purpose-built settings and resources to help your organization meet these requirements with confidence. Watch this hands-on webinar where our experts cover:
- Where compliance matters most and what’s changing — An overview of the regulatory landscape for healthcare and life sciences organizations, including FDA 21 CFR Part 11 and EU Annex 11 requirements for electronic records, as well as HIPAA requirements for handling protected health information (PHI).
- How to configure Acrobat Sign for your compliance needs — A live walkthrough of both Sign’s Bio-Pharma settings and configuration for HIPAA readiness with PHI data. Then, see these settings in action through a simulated clinical trial e-signature workflow from sender to signer.
- What resources are available to support your compliance journey — A tour of Sign’s rich compliance resources, including handbooks and white papers, the validation template package, and additional tools to help your team get started.
Whether you’re an IT admin configuring Sign for a regulated department or a compliance lead evaluating e-signature readiness, you’ll leave with a clear path to setting up Acrobat Sign for your healthcare, life science, or FDA-regulated workflows.
At a glance
Product: Acrobat Sign
Role: Admin,Developer,Leader,User