Courses #FDA - Eventura World us

Good Manufacturing Practices (GMP) 101

FDA Inspections Seminar for 2024

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

Supplier And Contract Manufacturer Management

SaMD Masterclass - Validation, Change Management, Cybertechnology, and Best Practices

3 Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries

Handling OOS Test Results and Robust Investigations

The Transfer Of Validated Methods

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

Analytical Instrument Qualification and Excel Validation - Preparing for FDA Audits

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

How To Ace An FDA Meeting - Preparation And Conduct

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