IP assignment agreements, licensing deals, CRO contracts, grant agreements, and regulatory documents — signed with compliant e-signatures for biotech companies at every stage.
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Technology transfer agreements, patent licences, research collaboration agreements, material transfer agreements, and IP assignment documents — all executed with legally binding e-signatures and court-admissible audit trails.
Patent licences, MTAs, technology transfer, and IP assignments for biotech companies.
Contract research organisation (CRO) agreements, research collaboration contracts, confidentiality agreements, and data sharing agreements — managed with Zignature's e-signature workflows.
CRO agreements, research collaborations, and data sharing contracts for biotech.
IND applications, BLA/NDA submissions, and regulatory correspondence often require documented authorisation signatures. Zignature provides the compliant e-signature infrastructure for biotech regulatory workflows.
Compliant e-signatures for regulatory submission authorisation documents.
From simple agreements to complex multi-party workflows.
No training required. Send your first document today.
IP assignment, CRO, collaboration, and regulatory document templates set up.
Academic, CRO, and partner signatories added with role-based fields.
Documents dispatched and signed without slowing R&D timelines.
Complete IP and regulatory document archive with audit trails.
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Everything you need to know.
Yes. Patent licence agreements — exclusive, non-exclusive, sublicenseable — are routinely executed via e-signature. Zignature's audit trail provides the execution evidence required for USPTO recordal and licensing program management.
Yes. MTAs for biological materials, cell lines, plasmids, and research reagents are commonly executed via e-signature. The signed MTA with audit trail provides the legal record of material transfer obligations.
Yes. Zignature can be used for the signatory authorisation documents accompanying regulatory submissions. The signed document and audit trail provide evidence of the authorised signatory's approval for submission.
Configure multi-party signing for university-industry research collaboration agreements — technology transfer office signatory, PI, industry sponsor, and legal counsel can all sign their respective sections with role-specific fields.
Yes. Zignature's authentication and audit trail architecture meets the core 21 CFR Part 11 requirements for biotech electronic records. Formal system validation should be conducted per your QA procedures.
Yes. NIH grant agreements, SBIR/STTR awards, and DOD research contracts can all include e-signed authorisation documents via Zignature, subject to the agency's e-signature acceptance policies.