Bizzmine, quick and efficient for Carbogen Amcis

Our production and its facilities need to meet the high standards of pharmaceutical production legislation. Within the quality system, Deviation Management, CAPA Management (corrective action and preventive action), Management of Complaints, and Management of Change (MoC) are important processes that have to comply with cGMP, ISO, and FDA requirements. In the past, these processes were managed in a paper-based system. The BizzMine workflow module has made the CAPA and MoC processes ‘paperless’ and compliant with the requirements of 21 CFR Part 11 (Electronic Records; Electronic Signatures).