Setting Up and Implementing Supplier Audits

December 23, 2015

CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
February 4, 2016 at 11:00 a.m.–12:30 p.m. (ET)

Who Should Attend?
This 90 minute accredited training will be of value to those professionals in the pharmaceutical, medical device and related industries who are responsible for or involved in any interaction with suppliers, including those in the following functions:

  • Management
  • Auditing
  • QA/QC
  • R&D
  • Manufacturing
  • Regulatory affairs
  • Laboratories
  • Purchasing
  • Procurement
  • Legal
  • Validation
  • Documentation management

Course Description

This course will present a brief overview of the outsourcing process in the FDA regulated industries with emphasis on the critical aspects of monitoring and preserving the integrity of the supply chain. The importance of risk management techniques will also be addressed. Details about steps to be taken by companies in setting up and implementing supplier audits will be discussed.

Can't Make this LIVE Webinar?
Simply select the On Demand option when registering and we will send you the link to view the recorded version.

This course will be available On Demand: February 5, 2016

Organized by:

CfPA-The Center for Professional Advancement

Invited Speakers:

Renée B. Galkin; Quality Management Consultant

Renée B. Galkin is a quality management consultant with over twenty years experience in the pharmaceutical and medical device industries. Her areas of expertise include quality audits, quality programs, FDA regulatory compliance, GMP training, documentation systems management, strategic planning and organizational development.

Prior to starting her own consulting business, Ms. Galkin held managerial positions with two major companies – Wyeth Pharmaceuticals, Inc. (now Pfizer) and Science Management Corporation (a multinational consulting firm). Throughout her career she had both domestic and international assignments.

Ms. Galkin holds an MBA in Business Management from New York University, an MA in Education from Brown University and a Bachelor of Science in Biology from Northeastern University. She is a member of the American Society for Quality, the Parenteral Drug Association and the International Society for Pharmaceutical Engineering (ISPE). As a consultant, Ms. Galkin provides training, auditing and compliance advisory services to companies worldwide. She also directs several technical courses offered by The Center for Professional Advancement.

Deadline for Abstracts:

n/a

Registration:

Please click here for registration information.

E-mail:

sberg@cfpa.com

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