This seminar will provide you with an understanding of the requirements for Quality Management Systems (QMS) for both the FDA and ISO 13485. You will understand how to create a Quality Management Systems that will comply with the requirements of both of these and how to add other country requirements, when desired. Reasons to attend: Understand where the FDA and ISO 13485 requirements come from Understand when each or both are needed and where there might be other quality system requirements Understand the details of the FDA Quality System Regulation and ISO 13485 requirements Understand how to create a compliant Quality Management System

Date : 7th August 2014 to 8th August 2014

Place : United States, Phoenix

Website :http://complianzworld.com/SeminarDetails.aspx?TopicId=8&Cotn=1324&Sub=Medical-Device-Quality-Management-Systems-and-CAPA-%E2%80%93-2-day-In-person-seminar

Contact Person:complianzworld

Description:

This seminar will provide you with an understanding of the requirements for Quality Management Systems (QMS) for both the FDA and ISO 13485. You will understand how to create a Quality Management Systems that will comply with the requirements of both of these and how to add other country requirements, when desired. Reasons to attend: Understand where the FDA and ISO 13485 requirements come from Understand when each or both are needed and where there might be other quality system requirements Understand the details of the FDA Quality System Regulation and ISO 13485 requirements Understand how to create a compliant Quality Management System

This seminar will provide you with an understanding of the requirements for Quality Management Systems (QMS) for both the FDA and ISO 13485. You will understand how to create a Quality Management Systems that will comply with the requirements of both of these and how to add other country requirements, when desired. Reasons to attend: Understand where the FDA and ISO 13485 requirements come from Understand when each or both are needed and where there might be other quality system requirements Understand the details of the FDA Quality System Regulation and ISO 13485 requirements Understand how to create a compliant Quality Management System will be held in Phoenix,United States on date 2014-08-08

---

Deadline for abstracts/proposals : 7th August 2014

Keynote Speakers :

Check the event website for more details.