Courses #Medical Device - Eventura World

OOS And OOT Investigations Course - Best Practices, Key Components and A Comprehensive Review of The FDA Requirements

The FDA's Qualification of Medical Device Development Tools (MDDT) Program

How To Ace An FDA Meeting - Preparation And Conduct

Risk-Based Excel Spreadsheet Validation

Data Integrity – In Compliance with CSA, 21 CFR Part 11, SaaS/Cloud, EU GDPR

Effective Internal Audit Program

Post-CSA Transition - Key Challenges And Leveraging Opportunities

Cybersecurity In Medical Devices Latest Guidance: Quality System Considerations And Content Of Premarket Submissions

Conducting Successful Complaint Investigations In Regulated Industries

Data Integrity For In Vivo Bioavailability And Bioequivalence (BA/BE) Studies

Statistical Methods For Process Validation

EO Sterilization Validation / Revalidation Per ISO 11135

1
2
3
4
5
6
»