Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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Webinars

Powerful Closed-loop CAPA - Meeting FDA Expectations

John E Lincoln
Sep 28, 2022

Good Laboratory Practices by Using The Quality Management System (QMS)

John Fetzer
Oct 12, 2022

The 6 Most Common Problems in FDA Software Validation and Verification

David Nettleton
Oct 13, 2022

Assess Impact For Supplier Change Notices

Alan M Golden
Oct 20, 2022

Structuring and Conducting Risk-Based Internal cGMP Compliance Audits

John E Lincoln
Oct 26, 2022

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

David Nettleton
Nov 3, 2022

Validation Sampling Plans

Alan M Golden
Nov 10, 2022

Cybersecurity and US FDA Requirements

John E Lincoln
Nov 16, 2022

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

David Nettleton
Dec 13, 2022

Seminars

Statistical Techniques for Medical Devices and Diagnostics

Virtual Seminar | September 28-29, 2022

21 CFR Part 11 Compliance for SaaS/Cloud Applications

David Nettleton
Virtual Seminar | October 4-5, 2022

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

David Nettleton
Virtual Seminar | October 4-5, 2022

Analytical Instrument Qualification and System Validation

Mark Powell
Virtual Seminar | October 27-28, 2022

Recordkeeping and Documentation in a GLP Laboratory (US FDA, US EPA and OSHA Focus)

John Fetzer
Virtual Seminar | October 27-28, 2022

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