Courses - Eventura.site

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

Steam Sterilization Microbiology and Autoclave Performance Qualification

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

3-Hour Virtual Seminar on 510(k) and PMA Submissions Process

Packaging and Labeling in Pharmaceutical Product Development – Best Practices

GOOD CLINICAL PRACTICES REVIEW OF ICH E6

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