industry solutions / life sciences
Life sciences organisations operate under the strictest document compliance requirements in any industry. Clinical trial agreements, regulatory submissions, GxP-controlled documentation, and commercial contracts, Doctavian governs every stage with the precision and audit rigour the industry demands.
ACROSS THE FULL VALUE CHAIN
Clinical trial agreements, investigator site contracts, and informed consent documentation generated from controlled templates, audit-ready and signed digitally without slowing trial timelines.
Regulatory submissions, GxP-controlled SOPs, and quality documentation managed with version control and enforced approval workflows, traceable at every stage of development.
Supplier qualification agreements, CMO contracts, and batch record sign-offs governed in a central repository, with role-based access and a tamper-proof audit trail on every document.
HCP engagement agreements, market access contracts, and distribution documentation generated at commercial speed, accurate, compliant, and signed before the opportunity passes.
FROM CLINICAL TRIAL TO COMMERCIAL LAUNCH
Clinical trial agreements and informed consent documents generated from pre-approved, audit-ready templates
GxP-controlled document workflows with enforced approval chains and full version history
eIDAS-compliant digital signatures on investigator, supplier, and commercial agreements
Regulatory submission documentation archived with tamper-proof audit trail and instant retrieval
Commercial and HCP agreements governed with renewal tracking and centralized repository access
FASTER DOCUMENTS, FASTER BREAKTHROUGHS.
1
Clinical, regulatory, and commercial documentation generated from controlled templates and live system data, accurate, GxP-aligned, and audit-ready from first draft.
2
eIDAS-compliant signatures at all three levels. Investigators, suppliers, and commercial partners sign from any device with a legally binding, tamper-proof record on every agreement.
3
Every contract across the R&D, manufacturing, and commercial lifecycle managed in one repository with version control, approval workflows, and automated renewal tracking.
4
Intelligent review of supplier, CMO, and commercial agreements. Non-standard clauses and compliance risks identified before execution without manual document review.
5
Connect Doctavian to your CTMS, LIMS, ERP, and CRM platforms via REST API or native integrations — triggering document workflows automatically from the systems your teams already use.
