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Introduction to Pharmaceutical Quality Management System

 
  August 20, 2019  
     
 
CfPA-The Center for Professional Advancement, Online Live
October 24, 2019 at 11:00 a.m.–12:30 p.m. (ET)


Who Should Attend?
This webinar will benefit various industries such as the Pharmaceutical, Biotechnology, Drug, Biologics, Medical Device and In-vitro Diagnostics Product Manufacturing Industries, especially those within various departments such as Quality Assurance Personnel and Management, Quality Control Personnel and Management, Laboratory Managers, Testing Analysts and Technicians, Manufacturing Personnel and Management, Supplier Quality Assurance Personnel and Management, Regulatory Affairs Personnel and Management, Shipping and Receiving Personnel and Management, Facility and Maintenance Personnel and Management, Microbiologist Personnel and Management, Engineering Personnel and Management, Materials Management Personnel and Management.

Course Description
This 90-minute accredited online training course describes the requirements of an effective, comprehensively designed and correctly implemented Pharmaceutical Quality Systems (PQS) that incorporates Good Manufacturing Practice, Controls, Continuous improvements and Quality Risk Management. All parts of the PQS should be adequately resourced with competent personnel, suitable and sufficient premises, equipment, facilities, processes and effective procedures. This course is for employees that have been introduced to the basic cGMP concepts who are in need of a deeper exposure to comprehensive Pharmaceutical Quality Systems requirements in the Pharmaceutical Industry per ICH Q10. 

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.

On Demand available approximately 3 business days after the live offering.
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Charity Ogunsanya, (Owner/CEO), Pharmabiodevice Consulting LLC

Charity Ogunsanya has more than 28 years of extensive experience within the Biologics, Pharmaceuticals, Radiopharmaceuticals, Biotechnology and Medical Device Industries and has been the Microbiology, Sterility Assurance, Contamination Control, Aseptic processing, Quality Control Subject Matter Expert (SME) for multiple fortune 100 companies.

She has a Bachelor of Science degree in Microbiology from the University of Benin-Nigeria and has a Masters degree from the Advanced Academic Master’s Biotechnology Program at the Johns Hopkins University with concentration in Biotechnology/Biodefense. She is the CEO/ Owner of her consulting firm named Pharmabiodevice Consulting LLC. Her consultancy provides support to Biologics, Pharmaceuticals, Radiopharmaceuticals, Biotechnology and Medical Device Industries.

 


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