Business type
Manufacturer

Areas of operation
All regions

Company description
Camstar’s InSite | Medical Device Edition solutions is fully FDA Regulation 21 CFR Part 11 compliant for Electronic Records and Electronic Signatures and Current Good Manufacturing Practices (cGMP) outlined by the FDA in 21 CFR Part 820. InSite | Medical Device Edition provides paperless eDHR device history record, and includes tightly integrated enterprise Corrective and Preventive Action (CAPA) functionality.