Date :
Place : United States, las vegas, nv
Website :http://www.mentorhealth.com/control/globalseminars/~product_id=200069SEMINAR
Contact Person:Event Manager
Description:
Overview: This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance. This course's aim is to prove "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts. It will teach participants to evaluate its elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management. Quick Contact: NetZealous DBA as MentorHealth Phone: 1-800-385-1607 Email: [email protected] Website: http://www.mentorhealth.com/ Registration Link - http://www.mentorhealth.com/control/globalseminars/~product_id=200069SEMINAR Follows us: Twitter: https://twitter.com/MentorHealth1 LinkedIn: https://www.linkedin.com/company/mentorhealthDeadline for abstracts/proposals : 7th June 2016
Organized By :Netzealous -MentorHealth
Keynote Speakers : John E Lincoln is Principal of J. E. Lincoln and Associates LLC, a consulting company. John, a graduate of UCLA, is a medical device and Regulatory Affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management and U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and have been descr
Conference Highlights :Senior and middle management and staff Regulatory Affairs Quality Assurance or Quality Control Professionals QA/QC IT/IS R&D Production Management Manufacturing Engineers Process Engineers Software Engineers Project Managers Hardware and software vendors, sales and marketing Any professional tasked with V&V responsibilities
Venue :Las Vegas, NV, United States
Check the event website for more details.