Courses #webinar - Eventura World us

FDA vs Health Canada - Similarities and Differences between the two Regulatory Bodies

Production and Process Controls for Medical Devices

EU's New Regulation 535/2014 On Clinical Trials - Insights Into Effective Clinical Trials

Good Clinical Practices Review of ICH E6 (R3) Latest Guidance

Continued Process Verification and Process Monitoring

FDA/ICH Guideline Q9 (R1) On Quality Risk Management

3-Hour Virtual Seminar On IEC 62304 - Medical Device Software Compliance

How to Deal with Bad Results Under GLP

Medical Device Hazard Analysis following ISO 14971

Auditing Computer Systems for Part 11 and International Compliance

Handling Out-of-Trend Results in Pharmaceutical Quality Control as per Latest FDA Requirements

Secrets to Writing Effective SOPs for QMS

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