DocuSign for Life Sciences
The World's #1 Way to Sign Electronically.
Overview
DocuSign is a global leader in electronic signatures. For the life sciences industry, they offer specific functionalities and controls to help organizations meet stringent regulatory requirements, including FDA 21 CFR Part 11. This allows DocuSign to be used for regulated processes like informed consent, SOPs, and other GxP documentation, providing a compliant, auditable, and widely trusted signature solution.
✨ Key Features
- 21 CFR Part 11 compliant module
- Signature-level credentialing
- Pre-packaged validation documentation
- Detailed audit trails
- Integration with a wide range of business systems
🎯 Key Differentiators
- Market leader with strong brand recognition and trust
- Specific compliance module for 21 CFR Part 11
- Extensive library of integrations
Unique Value: Provides a globally recognized, trusted, and compliant e-signature platform that can be readily deployed for regulated use cases like informed consent.
🎯 Use Cases (4)
✅ Best For
- Remote and on-site document signing for regulated processes
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Organizations needing a full clinical trial management suite (e.g., EDC, eISF)
🏆 Alternatives
Unlike specialized eConsent platforms, DocuSign is a horizontal tool that can be used across the entire organization for any signing need, but with the necessary controls for research compliance.
💻 Platforms
✅ Offline Mode Available
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Live Chat
- ✓ Phone Support
- ✓ Dedicated Support (Enhanced Plans tier)
🔒 Compliance & Security
💰 Pricing
✓ 30-day free trial
Free tier: Limited number of envelopes per month.
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