Docusign for Life Sciences
Accelerate discovery. Simplify compliance.
Bring life-changing therapies to market faster with a trusted platform for secure, compliant, and automated agreement management.
Accelerate discovery. Elevate quality. Expand market reach.
- Accelerate research and clinical development
Drive critical advances and get innovations to market faster with agreement automation, reducing 40% of personnel time per agreement.*
- Modernize manufacturing and quality
Build trust and ensure quality with secure, compliant agreements across your manufacturing operations, reducing compliance incidents by 19% and improving data quality by 95%.*
- Enhance commercial effectiveness
Streamline sales, market access, and HCP engagement while delivering personalized experiences driven by agreement AI. Accelerate transactions with unparalleled speed, with 76% completed in less than 24 hours.
How do life sciences organizations use Docusign?
Docusign IAM offers a single platform for every agreement that empowers life sciences organizations to transform agreements from bottlenecks to strategic drivers across the entire value chain, accelerating the journey of life-saving therapeutics from R&D to commercialization.
- Research and clinical development
Preclinical and clinical development
Clinical trial enrollment
Regulatory submissions
Investigator onboarding and site initiation
- Manufacturing and quality
GxP document management
SOPs, batch records, and more
Supplier qualification and onboarding
CMO and technology transfer agreements
- Commercial effectiveness
Sales contracting
Market access agreements
HCP engagement and speaker programs
Patient assistance and reimbursement
Ready to simplify compliance and boost efficiency?
IAM for life sciences
Centralize and automate the entire agreement lifecycle, integrating seamlessly into your R&D, quality, manufacturing, and CRM systems while ensuring compliance with the FDA 21 CFR Part 11 regulations.
Create
• Generate documents with pre-approved clauses
• Auto-ingest and classify documents
• Dynamic web forms for data capture
Commit
• Intuitive eSignature on any device
• Part 11-compliant signing with SMS authentication
• Centralized workspaces for tracking tasks and milestones
Manage
• 1,000+ integrations for seamless data flow
• Real-time reporting, analytics, and compliance tracking
• Ongoing monthly validation reports
Additional products and features for life sciences
FDA Part 11 Module
CapabilitiesSupport compliance with the U.S. Food and Drug Administration’s 21 CFR Part 11 regulations.Contract Lifecycle Management
ApplicationsManage contracts better with document generation, collaboration tools, automated workflows, and a searchable repository.
FDA Part 11 Module
Contract Lifecycle Management
Compliance and security you can trust
FDA 21 CFR Part 11-ready
Docusign Life Sciences Module is designed to help you meet global regulatory requirements, including FDA 21 CFR Part 11, GxP, and other industry standards.
Audit trails
Every agreement is tracked with a complete, automated audit trail and certificate of completion, providing transparency and accountability.
Enterprise-grade security
Docusign meets rigorous security standards, including SOC 2 Type 2 and ISO 27001, with industry-standard 256-bit encryption and PKI digital sealing to protect documents in transit and at rest.
Data privacy
Protect patient and organizations data with robust encryption, privacy controls, and data management practices. Docusign supports compliance with HIPAA, CCPA, GDPR, and other privacy regulations.
Featured integrations for life sciences
With 1,000+ prebuilt integrations to the tools your organization uses every day, break down data silos and connect every step of your agreement process to work more efficiently.
eSignature for Salesforce
IntegrationsBy DocusignSend, sign, and succeed with the world’s #1 eSignature solution and the world’s #1 CRM, together.
eSignature for Microsoft PowerAutomate
IntegrationsBy DocusignAdd eSignature tasks to your Power Automate workflows to simplify sending, signing and archiving agreements.
box for Docusign
Extension AppsBy DocusignThe Box extension app makes it easier for you to store files in your Box as part of an agreement flow.
eSignature for Salesforce
eSignature for Microsoft PowerAutomate
box for Docusign
Docusign for life sciences FAQs
In the life sciences industry, electronic signatures are used to streamline agreements. Pharmaceutical organizations use e-signatures for clinical trial enrollment, supplier contracts and more to accelerate the development and delivery of therapeutics to market. Medical device manufacturers use e-signatures for clinical testing, sales contracts, service agreements and more to accelerate product development and commercialization.
Docusign eSignature was the first e-signature tool to enable compliance with the FDA 21 CFR Part 11. Recently to meet the needs of our life sciences customers without jeopardizing compliance, we released a new package of features. The Life Sciences Pro package includes Part 11-specific eSignature functionality, Validator for Life Sciences, and SMS authentication. In the same way that Docusign was the first to offer Part 11 compliance, we’re the first to bundle features like this together for our life sciences customers.
The Life Sciences Module provides a high-availability, high-security, and highly customizable solution to maintain compliance with regulations domestically and globally. The module is designed to be incorporated as part of an open system solution, in which there is electronic communication among multiple parties and system access needs to extend to internal and external parties. This module is absolutely critical for any life sciences organization that handles electronic records.Learn More About Docusign's Life Sciences Module for 21 CFR Part 11
Docusign IAM empowers life sciences organizations to transform agreements from bottlenecks to strategic drivers across the entire value chain, accelerating the journey of life-saving therapeutics from R&D into manufacturing and through commercialization. By leveraging a single, extensible platform to manage all end-to-end agreement processes with unparalleled scale and trust, life sciences organizations see a 40% reduction in personnel time per agreement, a 19% reduction in compliance incidents, and a 95% improvement in data quality. Our unmatched ecosystem of 1,000+ integrations and robust APIs enables life sciences organizations to reduce risk, maintain compliance with evolving regulations, and ultimately unleash the power of their agreements for growth, innovation, and efficiency.
Ready to make your organization faster, simpler and more cost-efficient?
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Source: Paradoxes Inc., Industry Benchmark Research Study