Life sciences firms are grappling with the need to manage greater and greater volumes of documents, while maintaining a ‘single view of the truth’ for consistency and compliance concerns.
NextDocs streamlines inefficient, paper-based systems to shorten time to market and mitigate risks. By automating routing SOPs, DHF, DMR, and other documentation; obtaining approval and signatures; and manual search and retrieval of documents during FDA inspections, NextDocs ensures compliance, increases efficiency and reduces costs.
NextDocs connects various quality management processes, reduces cost of validation by automating labor-intensive validation tests conducted by internal staff and helps reduce exorbitant consultant fees which can easily double a company’s compliance costs.
Solutions for Pharmaceuticals, CRO’s, Medical Devices and BIO tech industries are readily available including:
- Clinical Trial Document Management
- SOP & Employee Record Document Management
- Quality Management
- Regulatory Document Management
- Project Document Management