ComplianceOnline

In this V&V planning webinar, you will learn to create a Master Validation plan, evaluate its elements against ISO 14971, ICH Q9 for hazard analysis and risk management, and understand how to employ DQs, IQs, OQs and PQs.

This 90-minute webinar will review FDA warning letters in Clinical Trials and present critical parameters to watch out for in order to secure compliance whether you are running or monitoring a clinical trial.

This 90-minute GCP webinar will present the official GCP text instead of interpretations of the GCP guidelines.

This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this, will translate GCP in a more practical, applied sense.

This webinar will outline common GCP violations and site mistakes found during a FDA investigator site inspection/audit and provide tips on how to avoid them.

This training on Adverse Event Reporting in Clinical Trials will show how to accurately observe and report AEs and SAEs, avoid common mistakes in AE / SAE reporting and successfully clear an FDA audit.

This 6-hr Clinical Project Management training will provide valuable tools and practical tips for initiating, managing, and presenting data from clinical projects. It will cover issues in clinical trial operations and site management.

This webinar will focus on the principal investigator's role and responsibilities, the legal language of FDA form 1572 or Device equivalent and how you can ensure a clean audit by following GCP.

In this GCP compliance webinar learn how to prevent and handle protocol deviations and violations

This training on managing employee healthcare costs will demonstrate proven health care demand management techniques, self-care programs and legal implications.