Quality management software for lifescience of Qualityze enables you to complain about internal and external regulations which has a closed loop EQMS system. This software enables you to comply with US FDA (21 CFR part 11, 21 CFR part 820), ISO 13485 standards, Pharmaceuticals and Medical Devices Agency (PMDA), and Therapeutic Goods Administration (TGA).
Quality is considered as the heart of every lifescience industry. In order to maintain the highest quality levels, companies should prevent chain disruption and minimize the operational hazards. Also they must eliminate the quality failures and avoid technology breakdown. As this Quality Management Software for Lifescience has an effective system, you can track every complaint’s lifecycle from documentation to initiation, investigation to reporting till its final closure to ensure that no further loopholes exist.
