Seminar on Internal Auditing for the Medical Device Industry

Overview:

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.

Who Will Benefit:

• Quality Manager
• Quality Associate
• Quality Engineer
• Quality Technician
• Regulatory Associate

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.

Location: SFO, CA Date: May 19th & 20th, 2016 Time: 9:00 AM to 6:00 PM

Venue: WILL BE ANNOUNCED SOON

Price: $1,295.00 (Seminar for One Delegate)

Register now and save $200. (Early Bird)

Until April 20, Early Bird Price: $1,295.00 from April 21 to May 17, Regular Price: $1,495.00

Quick Contact:

NetZealous DBA as GlobalCompliancePanel

Phone: 1-800-447-9407

Fax: 302-288-6884

Email: support@globalcompliancepanel.com      

Website: http://www.globalcompliancepanel.com/

Registration Link - http://bit.ly/medical-device-industry-SFO