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

Seminar: Future Trends in Content Management for Life Science and Chemical Companies Join your colleagues to discuss future trends in Documentum, in a seminar hosted by Generis and OSTHUS in the NH Mediapark Hotel in Cologne, Germany, on 3rd November 2015.  The seminar is free to attend but spaces are limited, so early registration is advised.  Guest speakers will be Oliver Mende and Tobias Bock from Bayer and Marie-Luise Schienstock from UCB. The agenda will include: 09:00 –