Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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Webinars

Reviewing Drug Product Batch Records

Mark Powell
Jul 16, 2020

Corona Virus - 19: New Risks with FDA Imports Logistics

Casper Uldriks
Jul 9, 2020

Batch Record Review and Product Release

Danielle DeLucy
Jul 9, 2020

GXP: Quality Standards and Regulations for the Medical Device Field

James W Monroe
Jul 10, 2020

Implementing a Robust Data Integrity Program

Kelly Thomas
Jul 13, 2020

Good Documentation Guideline (Chapter <1029> USP)

Afsaneh Motamed Khorasani
Jul 14, 2020

Supplier Management with the new Medical Device Regulation EU MDR 745/2017

Frank Stein
Jul 16, 2020

Best Practices in Preparation for an FDA Computer System Audit

Carolyn Troiano
Aug 27, 2020

21 CFR Part 11 and QMS Software Risk-Based Implementation

John E Lincoln
Dec 16, 2020

Seminars

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

Mark Powell
Virtual Seminar | July 6-7, 2020

Data Integrity: FDA/EU Requirements and Implementation

Mark Powell
Virtual Seminar | July 9-10, 2020

A Comprehensive View of FDA Regulations for Medical Devices

Stephanie Harrell
Tampa, FL | July 16-17, 2020

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

Barry A Friedman
Virtual Seminar | July 16-17, 2020

Quality Control Laboratory Compliance - cGMPs and GLPs

Kelly Thomas
Virtual Seminar | July 16-17, 2020

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

Rita Hoffman
Virtual Seminar | July 22-23, 2020

Biostatistics for the Non-Statistician

Elaine Eisenbeisz
San Francisco, CA | July 23-24, 2020

Design Control Essentials for Medical Devices

Susanne Manz
Virtual Seminar | July 23-24, 2020

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