This web seminar presents an overview of FDA’s Adverse Event Reporting Systems for Drugs and Medical Devices. Adverse Event Reporting for Investigational ...
This web seminar presents an overview of FDA’s Adverse Event Reporting Systems for Drugs and Medical Devices. Adverse Event Reporting for Investigational ...
The seminar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, calibration, and "uncertainty ...
FDA’s applies U.S. regulatory requirements to foreign manufacturers during an inspection under strict time constraints. A successful inspection requires thorough preparation and ...
This webinar is a must for those personnel that require an understanding of the regulation governing manufacturing operations. FDA’s regulates the manufacture ...
This 90 minute in-depth webinar discusses the FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name device ...
This 1 hour virtual seminar will help you understand compliant issues researchers face while conducting clinical trials especially in the drug trials. ...
This webinar will discuss the Part 11 requirements and practical techniques for evaluation of the current compliance status of a given organization. ...
Document! Document! Document!Don’t Let Inadequate Employee Documentation Cost You in Court.Workplace litigation is at record high levels. The average lawsuit settlement is ...
Current regulations expect that all users are appropriately trained and that must include being trained how to effectively perform UAT.This course provides ...
Compliance Trainings is the global organization for regulatory affairs professionals for those who have an interest in regulatory affairs in Food, drugs, ...