Courses #seminar - Eventura.site

FDA’S Latest UDI Labeling Requirements

Writing Validation Master Plans – Best Practices for Writing a Compliant Document

Analytical Instrument Qualification & Validation - Use of Excel and FDA Audit Preparation

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

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

The DHF, Technical Documentation - Similarities, Differences and the Future

Risk based approach to GxP Compliant Laboratory Computerized Systems

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