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Regulatory Impact on the Management of Pharmaceutical Contract Manufacturers (CMO’s): FREE WEBINAR

 
  January 18, 2018  
     
 
CfPA-The Center for Professional Advancement, FREE WEBINAR
February 6, 2018 at 11:00 a.m.–11:30 a.m. (ET)


Who Should Attend?
This informational webinar will provide insight to Pharmaceutical, Biotechnology, and Medical Device personnel on the principal US and EU regulatory requirements concerning manufacturers and their contractors.

It will be valuable to the following professionals:
  • Supply Chain
  • Quality Assurance
  • Manufacturing/Operations
  • Project Managers
  • Managers of “virtual” organizations
  • Regulatory Affairs

Course Description
Outsourcing operations to CMO’s has become a critical segment of nearly every pharmaceutical company’s strategy. Understanding the principal regulatory requirements is critical in developing a successful technical and contractual relationship. This 30-minute, informational webinar is designed to provide the attendee with a basic understanding of the applicable principals of US and EU regulatory requirements.

Can’t attend LIVE? Register anyway and we’ll send you a link to the webinar recording afterwards.

For complete coverage of this subject check our website for: 
Qualification and Management of CMO’s
April 17-18, 2018 | New Brunswick, NJ | Attend In Person or Virtually
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Frank Carroll, Carroll Pharma Consulting, LLC, Pharmaceutical Operations/Supply Chain

Frank Carroll is currently an independent pharmaceutical operations/supply chain consultant and Principal of Carroll Pharma Consulting, LLC. He has over 25 years’ experience in the Pharmaceutical, Device, Biologics, and Biotech industries in many aspects of operations including commercial and clinical product manufacturing and supply chain; purchasing; strategic alliance management; implementation of advanced project management systems; MRP/ERP systems; and senior operations management. He has held senior consulting positions at Pharmatech Associates and senior management positions at Zosano Pharma, Genitope Corp., Alpha Therapeutics, McGhan/Inamed Corp., Collagen Corp., and Bayer AG.

He has earned certifications from APICS (CPIM), ASQ (CQE), and Zenger-Miller as a certified trainer. He has instructed/directed numerous courses for the Center for Professional Advancement, instructed courses for APICS CPIM certification, and was a faculty member at Indiana University at South Bend in Continuing Education programs. He received his B.Sc. degree from The Ohio State University and MBA and MSBA degrees from Indiana University at South Bend. 

 


 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
 
   
 
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