Case Study: TriLink Biotechnologies achieves controlled document management in a GMP environment with Docsvault

TriLink Biotechnologies uses Docsvault for controlled document management after more than 2 years of use

TriLink BioTechnologies, a biotechnology company operating in a regulated GMP environment, needed a reliable document management solution to ensure quality, traceability, and compliance. Their challenge was to find a system that was intuitive for users, straightforward to administer, and provided strong value while supporting controlled document management processes. They evaluated solutions including Veeva QualityOne EQMS before selecting Docsvault.

Docsvault was validated under 21 CFR Part 11 and GAMP 5 for use in TriLink's GMP environment. The solution provided reliable performance, full document traceability, and an intuitive user experience. After more than two years of use, Docsvault has made compliance processes smoother and more efficient, performing exactly as intended. The system's stability and functionality have made it a dependable solution for managing controlled documents.

TriLink BioTechnologies