MEDICAL DEVICES TRAINING ON QSR AND ISO REQUIREMEN 2015 - A Bulletproof, Cost-Efficient Supplier Management Program

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Category FDA GXP Compliance - Medical Devices

Deadline: January 28, 2015 | Date: January 28, 2015

Venue/Country: Palo Alto, U.S.A

Updated: 2015-01-23 14:35:28 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

Supplier qualification and assessment is required according to both QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this.

Who Will Benefit:

This webinar will provide valuable assistance to all regulated companies that are interested in implementing a supplier management program that is both compliant and cost-efficient. The employees who will benefit include:

Purchasing management

Regulatory management

QA management

Consultants

Instructor Profile:

Jeff Kasoff, RAC, is the director of quality at Medivators, a leading manufacturer of endoscopy consumables and instrumentation. In this position, Mr. Kasoff is responsible for oversight of the quality system, including the CAPA program, and is the liaison with FDA. For 13 years prior to that, he served as director of regulatory affairs at Life-Tech, Inc., in which capacity he was similarly responsible for quality system oversight. Mr. Kasoff began his regulatory career as the first full-time employee of Optex Biomedical, a device start-up, where he initiated their regulatory policies and procedures and prepared their submissions. He received his Regulatory Affairs Certification in 1996.