Overview
SciNote provides a flexible electronic lab notebook (ELN) with built-in inventory management, compliance tools, and team collaboration features tailored for biopharma, cell therapy R&D, and industrial laboratories. It supports 21 CFR Part 11 compliance through electronic signatures, audit trails, and GLP/GMP requirements, enabling structured protocols, sample tracking, and chain-of-custody management. The platform integrates via robust APIs and webhooks, as demonstrated in case studies with FogPharma and Dynamic Code for streamlined workflows and quality management.
Frequently asked questions
- What compliance standards does SciNote support for pharma R&D?
- SciNote supports 21 CFR Part 11 compliance with electronic signatures, electronic witnessing, audit trails, and meets GLP/GMP requirements for regulated labs.
- What are the key capabilities of SciNote ELN for biopharma?
- SciNote ELN offers inventory management, sample tracking, protocol digitization, chain-of-custody, API integrations for real-time data, and scalability for cell therapy and biopharma R&D.
- In which geographies and sectors is SciNote used?
- SciNote serves government, industrial, academic, and biopharma labs globally, with case studies including Boston-based FogPharma and ISO 27001 certification for secure operations.