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Live Business Training Events
TBD
Live
Vendor Audit for Systems and Services for FDA Regulated Systems
Time: TBD | Duration: 90 minutes
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TBD
Live
ICH Q14 - Analytical Procedure Development Examination of the New Step 4 Guideline
Time: TBD | Duration: 120 minutes
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TBD
Live
AI in Drug Discovery: Aligning with FDA's Latest Risk-Based Framework
Time: TBD | Duration: 90 minutes
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Recording Business Training Events
Jun 19, 2023
Recorded
How to Validate FDA-Regulated Computer Systems in the Cloud 4 part series
Date: Jun 19, 2023 | 1:00 PM EST | Duration: 720 minutes
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Jul 14, 2023
Recorded
Excel Spreadsheets - Ensuring Data Integrity and 21 CFR Part 11 Compliance
Date: Jul 14, 2023 | 1:00 PM EST | Duration: 90 minutes
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Aug 16, 2023
Recorded
Human Error Reduction In GMP Manufacturing/Floor
Date: Aug 16, 2023 | 1:00 PM EST | Duration: 90 minutes
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Oct 04, 2023
Recorded
Analytical Method Validation and Transfer
Date: Oct 04, 2023 | 1:00 PM EST | Duration: 90 minutes
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Nov 08, 2023
Recorded
Aseptic Processing Overview and Validation
Date: Nov 08, 2023 | 1:00 PM EST | Duration: 90 minutes
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Nov 29, 2023
Recorded
Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submission
Date: Nov 29, 2023 | 1:00 PM EST | Duration: 90 minutes
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Jun 09, 2025
Recorded
Decision-Making and Human Error Prevention
Date: Jun 09, 2025 | 1:00 PM EST | Duration: 90 minutes
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Oct 14, 2025
Recorded
Analytical Methods, Process, Equipment, Cleaning, and Sterilization Validations Course
Date: Oct 14, 2025 | 1:00 PM EST | Duration: 90 minutes
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Oct 31, 2025
Recorded
FDA’s Final Rule for IRB Compliance: What You Must Know Now 2025 Update
Date: Oct 31, 2025 | 1:00 PM EST | Duration: 90 minutes
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Oct 31, 2025
Recorded
Changes to 21 CFR 820 - Device QSR to QMSR - Due February 02, 2026
Date: Oct 31, 2025 | 1:00 PM EST | Duration: 90 minutes
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Nov 20, 2025
Recorded
Implementing FDA Guidance for AI in Medical Devices: A Practical Approach
Date: Nov 20, 2025 | 1:00 PM EST | Duration: 60 minutes
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