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Welcome to Biofind events. Here we provide a list of events which have been registered with us, as well as a calendar view of upcoming events. If you want to post an event with us click here.

Event Location
A Comparison of ICH Q-10 Quality System and the FDA’s Quality Systems Approach (QSA) to the Pharmaceutical cGMPs More details
Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers More details
Recent Major Industry CGMP Failures More details
Practical Project Management for FDA-Regulated Companies More details
Design Control Explained for Medical Industry - Webinar By ComplianceOnline More details
Software Verification and Validation Planning and Execution - Webinar By ComplianceOnline More details
Don't RISK to ignore RISKS. Understanding ISO 14971 - Medical Device Webinar By ComplianceOnline More details
Risk-Based Verification and Validation Planning to Meet U.S. FDA, ICH Q9 and ISO 14971 More details
How to withstand an FDA audit of your facilities: A primer for clinical sites, manufacturing facilities and labs More details
Presenting the real GCP handbook: Build solid knowledge of GCP by learning the rules exactly as they appear in the official text More details
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