Courses - Eventura.site

Supplier And Contract Manufacturer Management

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

Is it a Drug, a Medical Device or both? Determine Product Classification with Precision and Risk

Handling OOS Test Results and Robust Investigations

Failure Investigation And Root Cause Analysis - Tools And Techniques

The Transfer Of Validated Methods

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

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

The Human Error Tool Box – A Practical Approach

510(k) Modernization, Breakthrough Device, and Safer Technologies Programs (STeP)

How to Deal with Bad Results Under GLP

TECHNICAL WRITING MASTERCLASS IN THE LIFE SCIENCES

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