CAPA Investigations - Tools for a Compliant and Effective Investigation Process Buy Now Section This training program will provide professionals with

This training program will provide professionals with essential elements of CAPA investigations to assure compliance with regulatory requirements. The corrective and preventive action (CAPA) program is an essential element of a compliant quality management system, as required by international regulations and voluntary standards.

Why Should You Attend:

A central theme in every CAPA investigation is determination of reoccurrence. Reoccurrence of deviations, non-conformances, or incidents may be indicative of inadequate investigations and/or ineffective identification of CAPAs. 

Who Will Benefit:

This CAPA investigations webinar will provide professionals from pharmaceutical, biotechnology, medical device and active pharmaceutical ingredient industries with the necessary tools to investigate non-conformances and deviations. It will be of interest to personnel directly involved in completing, reviewing or approving investigations. Expected participation by:

Quality Engineers

Manufacturing Engineers

Quality Systems Managers

Operations Managers

Instructor Profile:

Carlos A. Rodriguez-Garcia, PhD, ASQ CSSGB, CBA is president of BioMed Pharma Consulting, LLC, an independent consulting firm providing services in quality management systems to the pharmaceutical and medical industries. Mr. Rodriguez-Garcia has over 15 years of experience in the regulated industry, the vast majority in quality management, encompassing a wide scope of products and processes: plastics, parenterals and aseptic processes.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/capa-investigations-tools-for-a-compliant-and-effective-investigation-process-webinar-training-704039-prdw?channel=sciencedz