Boost efficiencies and reduce product development time

Bringing a drug to market already takes long enough. You can’t afford to waste critical time on inefficient processes like faxing and overnighting documents, which delay a patient’s access to the treatments you’re developing. That’s why 14 of the top 15 global pharmaceutical companies use DocuSign to improve the efficiency of clinical, quality, and internal operations. From patient consents to vendor contracts, DocuSign's eSignature solutions meet the needs of pharmaceutical organizations while supporting compliance with industry regulations like 21 CFR Part 11.


Expand your global reach

To serve a global patient population, you need to conduct trials and launch products in markets around the world. We’ve got you covered. DocuSign is available in 44 languages, and we have invested more than $500 million into our product to support customer needs worldwide.




Choose the most reliable and secure service

We work with industry experts to ensure our technology, people, and processes meet your security and compliance standards. DocuSign supports compliance with 21 CFR Part 11, HIPAA, eIDAS and EMA regulations, and more. We have the industry’s strongest data encryption practices, with systems audited and certified against the most rigorous security certifications like ISO 27001, TRUSTe, PCI, and SSAE 16. It's no wonder DocuSign is trusted by 14 of the top 15 global pharmaceutical companies.




We have the partners you need

We’ve worked hard to build relationships with life sciences industry partners like SAFE-BioPharma, Microsoft, Exostar, and USDM Life Sciences. DocuSign integrates with key technologies and validation partners to help you meet compliance requirements and stay fully digital.



Use Cases

DocuSign is used to complete documents, approvals and agreements in the pharmaceutical industry, including:

  • Patient informed consent
  • Label change requests
  • Electronic batch records
  • Clinical trial onboarding
  • Key Opinion Leader programs
  • Vendor contracts
  • Monitoring trip reports
  • Patient assistance documents
  • Sales agreements







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