Courses - Eventura World

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

Medical Device Hazard Analysis following ISO 14971

Top Process Validation Mistakes – And How to Avoid Them

Quality in Technology Transfer Projects

Auditing Computer Systems for Part 11 and International Compliance

Death by CAPA - Does your CAPA Program need a CAPA?

4-HOUR VIRTUAL SEMINAR ON CHANGE CONTROL ACCORDING TO GXP AND GMP REQUIREMENTS

WRITING EFFECTIVE STANDARD OPERATING PROCEDURE (SOPS) AND WORK INSTRUCTIONS (WIS)

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