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Achieving Compliance with Proper CAPA Systems for Medical Devices

 
  July 25, 2017  
     
 
CfPA-The Center for Professional Advancement, Online Live
August 17, 2017 at 11:00 a.m.–12:30 p.m. (ET)


Who Should Attend?
This online training will benefit professionals in the Medical Device Industry. It will be especially valuable to Senior Management and to Personnel and Management in the following areas:
  • Quality Control
  • Manufacturing 
  • Regulatory Affairs 
  • Quality Assurance 
  • Supplier Quality 

Course Description
This 90-minute accredited course will include discussions proper CAPA system maintenance, root cause analysis, documentation of the Corrective and Preventative Actions and developing a robust CAPA plan pertaining to the Medical Device Industry. It will give tips on how to develop CAPAs pertaining to longer term projects and ensure they stay on track.

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: August 18, 2017
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Danielle DeLucy, MS, Independent Consultant to the Biologics and Pharmaceutical Industries

Danielle DeLucy, MS, is currently an Independent Consultant to the Biologics and Pharmaceutical Industries specializing in the areas of Quality Assurance and Quality Systems. Prior to this role, Danielle has been in the industry for 15 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations. Danielle began her QA career as a Quality Control Pharmaceutical Microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the Quality management arena while increasing her responsibility. She has helped to lead many Regulatory Health Inspections and was instrumental in the coaching process of her peers prior to any inspection. Currently, Danielle assists companies who are faced with warning letters and consent decrees establish more robust quality systems so that the company can succeed.
 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
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