Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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Webinars

SaaS/Cloud Risk-Based Validation With Time-Saving Templates

David Nettleton
Jun 10, 2021

Calculations for Process and Product Capability

Elaine Eisenbeisz
Apr 15, 2021

Human Error Investigations, Root Cause Determination and CAPA Effectiveness

Ginette M Collazo
Apr 20, 2021

ISO 14971:2019 - Does your Risk Analysis meet this new revision of the Standard?

Betty Lane
Apr 22, 2021

Reviewing Drug Product Batch Records

Mark Powell
Apr 26, 2021

Implementing the 2021 Guidelines for Office and Outpatient Visits

Lynn M Anderanin
Apr 27, 2021

Good Documentation Practice and Record Keeping Regulations (FDA & EMA)

Afsaneh Motamed Khorasani
Apr 28, 2021

How to Achieve a Compliant and Effective Cleanroom Design and Facility Validation

Charity Ogunsanya
Apr 28, 2021

Is My Nanotechnology Safe? Approaches For NanoEHS Risk Assessments

Rob MacCuspie
Apr 28, 2021

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

David Nettleton
May 4, 2021

Seminars

21 CFR Part 11 Compliance for SaaS/Cloud Applications

David Nettleton
Virtual Seminar | April 28-29, 2021

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

David Nettleton
Virtual Seminar | April 28-29, 2021

Navigating the Medical Device Post-Market Maze and Challenges during COVID-19 Pandemic - Learn what FDA is really thinking on regulation and ....

Rita Hoffman
Virtual Seminar | April 29-30, 2021

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

Cynthia Brysch
Virtual Seminar | May 10-11, 2021

FDA Audit, Quality Assurance Practices, Responsibilities and Expectations

Virtual Seminar | May 20-21, 2021

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