Trainingknowledgehub - Your right platform for compliance training.

Industry: FDA Compliance

LiveWebinars

FDA QMSR Explained: How the QMSR Replaces the QSR

ins

By: Edwin Waldbusser | March 16, 2026

Duration: 60 Minutes | Time: 10:00 AM PDT | 01:00 PM EDT

FDA Regulation of Artificial Intelligence/ Machine Learning

ins

By: Edwin Waldbusser | March 25, 2026

Duration: 60 Minutes | Time: 10:00 AM PDT | 01:00 PM EDT

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026

ins

By: David Nettleton | March 25, 2026

Duration: 90 Minutes | Time: 10:00 AM PDT | 01:00 PM EDT

Recorded Session

Excel Spreadsheets; Develop and Validate for 21 CFR Part 11 Compliance

ins

By: David Nettleton | Recorded Session

Duration: 75 Minutes

FDA Compliance And Laboratory Computer System Validation

ins

By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)

ins

By: Kelly Thomas | Recorded Session

Duration: 90 Minutes

Human Factors Usability Studies Following ISO 62366 and FDA Guidance

ins

By: Edwin Waldbusser | Recorded Session

Duration: 60 Minutes

FDA Recommendations for Artificial Intelligence/Machine Learning (AI/ML)-Enabled Device Software Functions

ins

By: Rachelle D Souza | Recorded Session

Duration: 75 Minutes

Clinical Trial Systems: The Trial Master File (TMF) and Electronic Trial Master File (eTMF)

ins

By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

ChatGPT and Project Management: Leveraging AI for Project Management Excellence

ins

By: Charles H. Paul | Recorded Session

Duration: 90 Minutes

Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

ins

By: Kelly Thomas | Recorded Session

Duration: 90 Minutes

Writing Effective 483 and Warning Letter Responses

ins

By: Kelly Thomas | Recorded Session

Duration: 90 Minutes

21 CFR Part 11 - Compliance for Electronic Records and Signatures

ins

By: Edwin Waldbusser | Recorded Session

Duration: 60 Minutes

2-Hour Virtual Seminar on the 6 Most Common Problems in FDA Software Validation and Verification

ins

By: David Nettleton | Recorded Session

Duration: 120 Minutes

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

ins

By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

How to Prepare For and Host a FDA Inspection and Respond to 483's

ins

By: Edwin Waldbusser | Recorded Session

Duration: 60 Minutes

FDA Technology Modernization Action Plan (TMAP) and Impact on Regulated Computer Systems and Data Integrity

ins

By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

From Challenges to Compliance: Understanding Dietary Supplement Oversight by the FDA

ins

By: Meredith Crabtree | Recorded Session

Duration: 90 Minutes

SOPs - How to Write Them to Satisfy those Inspectors

ins

By: Meredith Crabtree | Recorded Session

Duration: 60 Minutes

Implementing an Effective Human Error Reduction Program

ins

By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

Performance of Root Cause Analysis, CAPA, and Effectiveness Checks

ins

By: Meredith Crabtree | Recorded Session

Duration: 90 Minutes

Zero Acceptance Sampling to Reduce Inspection Costs

ins

By: William A. Levinson | Recorded Session

Duration: 90 Minutes

Setting up Quality System for FDA Regulated Products: Tips and Tricks for your Regulatory Compliance

ins

By: Meena Chettiar | Recorded Session

Duration: 60 Minutes

Best Practices in Complaint Management for Regulatory Compliance and Customer Retention

ins

By: Jeff Kasoff | Recorded Session

Duration: 60 Minutes

Ensuring Safe and Effective Pharmaceutical Products: A Comprehensive Guide to ICH Q9 (R1) Quality Risk Management in the Pharmaceutical Industry

ins

By: Meredith Crabtree | Recorded Session

Duration: 90 Minutes

Supplier Management: Overcoming Challenges and Exploring Opportunities

ins

By: Jeff Kasoff | Recorded Session

Duration: 60 Minutes

Implementing a Robust Change Control Program - Key Elements for Process and Documentation Compliance

ins

By: Kelly Thomas | Recorded Session

Duration: 90 Minutes

21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA

ins

By: Carolyn Troiano | Recorded Session

Duration: 60 Minutes

Aseptic Process Validation: Top-Tips for Compliance and Success

ins

By: Kelly Thomas | Recorded Session

Duration: 90 Minutes

Analytical Method Validation and Transfer Course

ins

By: Kelly Thomas | Recorded Session

Duration: 90 Minutes

FDA Compliance and Clinical Trial Computer System Validation

ins

By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

FDA current recommendations related to timely initiation of and responses to recalls

ins

By: Meredith Crabtree | Recorded Session

Duration: 75 Minutes

How to implement an effective Human Error Investigation Program

ins

By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

Supervising a Human Error Free Environment: You can do a Lot More than you Think

ins

By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control

ins

By: Kelly Thomas | Recorded Session

Duration: 90 Minutes

Bad Standard Operating Procedures (SOPs) - Bad Training: Garbage In, Garbage Out

ins

By: Michael Esposito | Recorded Session

Duration: 90 Minutes

Data Governance for Computer Systems Regulated by FDA

ins

By: Carolyn Troiano | Recorded Session

Duration: 60 Minutes

FDA 21 CFR Part 11

ins

By: Willi Ramseier | Recorded Session

Duration: 60 Minutes

Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success

ins

By: Michael Esposito | Recorded Session

Duration: 90 Minutes

Data Governance for Computer Systems Regulated by FDA

ins

By: Carolyn Troiano | Recorded Session

Duration: 60 Minutes

FDA Case Scenarios - Best Practices for Managing Inspection Situations

ins

By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

Data Governance for Computer Systems Regulated by FDA

ins

By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

The FDA Inspection: Preparation, Performance and Follow-Up

ins

By: Jeff Kasoff | Recorded Session

Duration: 75 Minutes

FDAs Recent Clarification on Guidance for Managing Data Integrity for Regulated Computer Systems

ins

By: Carolyn Troiano | Recorded Session

Duration: 60 Minutes

Packaging and Labeling in Pharmaceutical Product Development - Best Practices

ins

By: Michael Esposito | Recorded Session

Duration: 90 Minutes

The 6 Most Common Problems in FDA Software Validation and Verification Computer System Validation Step-by-Step

ins

By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices

ins

By: Susanne Manz | Recorded Session

Duration: 90 Minutes

21 CFR Part 11 Conformance for Medical Devices

ins

By: Edwin Waldbusser | Recorded Session

Duration: 90 Minutes

FDA s New Import Program for 2019

ins

By: Casper E Uldriks | Recorded Session

Duration: 60 Minutes

Using Learning Management Systems (LMS) to Develop Pharma Training: Rewards & Challenges

ins

By: Michael Esposito | Recorded Session

Duration: 90 Minutes

Manufacturing and Marketing OTC Drugs in Compliance with FDA Regulations

ins

By: Dr. Loren Gelber | Recorded Session

Duration: 90 Minutes

FDA's Enforcement Strategy for Mobile Medical Applications

ins

By: J.Lawrence Stevens | Recorded Session

Duration: 60 Minutes

Food Safety And Quality In Home Food Delivery

ins

By: Dr. John Ryan holds | Recorded Session

Duration: 60 Minutes