Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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Webinars

US FDA Labeling Requirements for Medical Devices

John E Lincoln
Feb 8, 2023

GMP Compliance for Quality Control and Contract Laboratories

David L Chesney
Feb 20, 2023

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

David Nettleton
Feb 22, 2023

Medical Device Non-Product Software Validation Training

John E Lincoln
Feb 22, 2023

Medical Device Process Validation Training for Professionals

John E Lincoln
Feb 23, 2023

How to Create Clinical Evaluation According to EU MDR 2017/745 Article 61 and Annex XIV

Frank Stein
Mar 6, 2023

Conducting Remote Medical Device QMS Audits Training

John E Lincoln
Mar 8, 2023

Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

David Nettleton
Mar 14, 2023

Knowing your Post-Market Clinical Follow-up (PMCF)

Frank Stein
Mar 14, 2023

The Summary of Safety and Clinical Performance (SSCP)

Frank Stein
Mar 27, 2023

Seminars

Statistics for Process Control

Virtual Seminar | February 23, 2023

Statistical Elements of Implementing ICH Quality Guidelines

Elaine Eisenbeisz
Las Vegas, NV | March 16-17, 2023

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

Barry A Friedman
Philadelphia, PA | March 16-17, 2023

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

David Nettleton
Virtual Seminar | March 28-29, 2023

21 CFR Part 11 Compliance for SaaS/Cloud Applications

David Nettleton
Virtual Seminar | March 28-29, 2023

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