Generis CARA preconfigured for Medical Device documents based on the DIA Reference Model
CARA, Generis’ innovative and leading user interface for Documentum now assists Medical Device Companies in meeting FDA and other regulatory and quality requirements for the design, development and manufacture of Medical Devices, based on the DIA’s Reference Model. Regulators require that all providers, manufacturers and distributors of Medical Devices meet a stringent approval process and abide by rigorous quality standards before and after a Device is distributed. In additi