Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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Webinars

Medical Device Industry Trends for Computer Systems Regulated by FDA

Carolyn Troiano
Sep 28, 2020

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

David Nettleton
Sep 29, 2020

How to Investigate Environmental Monitoring Excursions

Gerry O Dell
Sep 30, 2020

The 6 Most Common Problems in FDA Software Validation and Verification

David Nettleton
Oct 27, 2020

How To Manage Supplier Compliance Through Automation

Jennifer Crandall
Nov 19, 2020

21 CFR Part 11 and QMS Software Risk-Based Implementation

John E Lincoln
Dec 16, 2020

Seminars

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

David Nettleton
Virtual Seminar | October 1-2, 2020

21 CFR Part 11 Compliance for SaaS/Cloud Applications

David Nettleton
Virtual Seminar | October 1-2, 2020

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection

Rita Hoffman
Virtual Seminar | September 24-25, 2020

Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines

Mark Powell
Virtual Seminar | October 8-9, 2020

FDA Recalls - Before You Start, and After You Finish

Casper Uldriks
Virtual Seminar | October 8-9, 2020

Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

Mark Powell
Virtual Seminar | October 19-20, 2020

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

Barry A Friedman
Virtual Seminar | November 5-6, 2020

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