Overview
The training provides insight into how to approach creating standard operating procedures that define the everyday business practices that comply with FDA regulations and International standards for quality management systems. In addition, you'll understand why you need to approach this as a responsibility of being in the medical device industry.
Why you should Attend
Areas Covered in the Session
Who Will Benefit
The training provides insight into how to approach creating standard operating procedures that define the everyday business practices that comply with FDA regulations and International standards for quality management systems. In addition, you'll understand why you need to approach this as a responsibility of being in the medical device industry.
Why you should Attend
- The importance of your Quality Management System being part of the business operations.
Areas Covered in the Session
- The medical device industry chose the Quality Management System (QMS) approach to doing business
- An effective QMS can be a desirable way of conducting business
- Having to implement a QMS and then have to explain reasons why to FDA is no way to conduct business; way to costly
Who Will Benefit
- Executives
- Managers and Quality Personnel
Speaker
Raymond M. Pizinger has over 30 years of hands-on professional experience in the fields of Best Business Practices, Quality Systems, Worldwide Regulatory Compliance and Submission, Quality Assurance, Engineering, Operation. Directed quality organizations through start-up, mergers, acquisitions, divestitures, IPO’s and OEM alliances. He has an extensive experience in the Medical Device Industry as an executive, consultant and international trainer.Who Should Attend
- Executives
- Managers and Quality Personnel
