Development Life Cycle Web-based Seminars

Effective Hazard Analysis to Meet FDA and ISO 13485 2003 Risk Management Requirements - Webinar By GlobalCompliancePanel Overview: FDA-GMPs, known as Quality System Regulations (QSRs), and ISO 13485 require Risk Management as integral part of the development life cycle. The starting point for each risk management lifecycle is the Hazard and Risk Analysis which provides safety critical design input for the device design. Price List: Live : $245. 00 Corporate live : $995. 00 Recorded : $295. 00  more...

Effective Hazard Analysis to meet FDA and ISO134852003 Risk Management Requirements - webinar by global compliance panel FDA-GMPs, known as Quality System Regulations (QSRs), and ISO 13485 require Risk Management as integral part of the development life cycle.  more...