Courses #FDA - Eventura World

3-Hour Virtual Seminar on cGMP Regulatory Inspections – Through the Eyes of FDA, EMA and PMDA

4-Hours Virtual Seminar – Medical Device Cybersecurity and FDA Compliance

Data Integrity and Privacy – compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

Step-by-Step approach for Setting up FDA Audit Ready Quality Management System (QMS) – Case Studies based training

Human Factors Engineering to Satisfy the New IEC 62366-1, -2

Packaging and Labeling in Pharmaceutical Product Development – Best Practices

Self Inspection Techniques - Avoid the most common and recent FDA observations

QUALITY & REGULATORY PATHWAYS FOR SAMD & AI DEVICES – ALL YOU NEED TO KNOW

21 CFR PART 11 DATA INTEGRITY TRAINING FOR SAAS/CLOUD, EU GDPR - HOW TO REDUCE COSTS FOR COMPLIANCE

A to Z of Supplier Management in the Medical Device Industry

Successful Deviation Investigations

FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices

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