Courses - Eventura World us

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

Human Error and Management Systems – Designing Errors Out

Document Controls for Medical Devices

Successful Deviation Investigations

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