Product Category

Trial Master File (TMF) – Clinical Trial Systems and FDA Expectations

Measurement, Analysis, and Improvement for safe and Effective Medical Devices

How to Prepare for and Host a FDA Inspection and Respond to 483’s

ISO 14971:2019 Medical Device Hazards and Risk Management – All you need to know

COVID-19 Update: Get Ready for the HEROES Act’s OSHA Requirements

Data Integrity and Privacy – compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

Introduction to Design of Experiments

3-Hour Virtual Seminar on Human Error Prevention in the Life Sciences

3-Hour Virtual Seminar on Complaint Handling and Medical Device Reporting and Recalls

Good Documentation Practices – What Helps Make Your Controlled Documents Compliant

Onboarding In A GMP Environment – Best Practices

Regulatory and Testing Requirements of the Bacterial Endotoxin Testing (BET) or LAL Progra

4-Hours Virtual Seminar – Medical Device Cybersecurity and FDA Compliance

FDA’s Latest UDI Labeling Requirements

Getting R&D on Board with Risk Analysis

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