GlobalCompliancePanel

This webinar concentrates on the value of creating a master plan for contamination risks within a GMP manufacturing company.

This webinar concentrates on identifying and discussing testing and certification requirements associated with cleanrooms.

Process Validation is required by FDA and most regulatory bodies. PV demonstrates consistency of pharmaceutical processes.

Although Part 11 has been around for over a decade, lack of visibility can sometimes render compliance with this regulation an afterthought.

Where business is concerned the world is becoming a smaller place.

This presentation will attempt to remove the fear of statistics that most people share. We will not spend much time on complex equations. Rather, we will focus on the concepts of statistics

This CAPA training program helps you to understand, in 10 easy steps, the entire CAPA process. It includes elements of Quality Tools, Team Effectiveness, Awards & Recognitions, and Verification & Validation of actions taken.

Much attention has been paid to the regulatory requirements of reprocessing SINGLE use devices. However, there is increasing attention being directed towards reprocessing REUSABLE medical devices and regulatory requirements.

Computerized systems can be a boon to the Sales and Marketing group of an organization that falls within FDA regulatory authority.

This presentation will assist organizations within the food chain to understand the requirements to meet the international standard for Food Safety Management.