This course provides an overview of internal auditing requirements and techniques for medical device companies as a method for risk management and quality improvement.
The course will cover auditing requirements, audit planning, preparation, knowledge, auditor skills, interviews, documents and records review, objective evidence, audit report writing and corrective action.
Why should you attend:
Attendees should attend this seminar for risk management and improvement purposes to identify weaknesses, problems, compliance risks, and improvement opportunities.
Speaker
Joseph Azary, Director Regulatory and Quality at Sekisui American Diagnostica
Joseph Azary has over 25 years of quality and regulatory experience in the medical device industry. Joseph is currently the Vice President of Quality Assurance & International Regulatory Affiars at Z-Medica, LLC.
Joseph Azary has worked for companies such as US Surgical (now part of Covidien), Johnson & Johnson, Fujifilm Medical, and Sekisui Diagnostics. Mr. Azary was a consultant for 10 years working with approximately 180 companies. He has sold his consulting company, Azary Technologies in 2008.
Joseph has a bachelors degree in Biological Science from University of Connecticut and a Masters of Business Administration (MBA) in public health from Sacred Heart University. Joseph is an ASQ Certified Quality Auditor (CQA).
Please fill in your name and email to receive the seminar agenda of this event.
The agenda is available as PDF under downloads at the right side of the page.
Venue
The venue is not yet available for this event.
Follow this event to be informed when the venue is available and stay informed on other changes.
Who will benefit:
- Quality Manager
- Quality Associate
- Quality Engineer
- Quality Technician
- Regulatory Associate
Venue
Venue to be confirmedSan Francisco, SFO, CA
