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Stability Operations for Drugs, Biologics and Medical Devices

 
  November 12, 2019  
     
 
CfPA-The Center for Professional Advancement, Edison, NJ or Virtually
March 16-17, 2020


Who Should Attend?
This course is designed to benefit professionals in the Pharmaceutical, Biological and Medical Device Industries who execute Stability Operations for their company. Stakeholders who support, rely or otherwise liaise with the stability function would additionally benefit in understanding the regulatory constraints of a stability operation. These include:
  • Stabilitarians and Product Stability Managers
  • Sample Control Specialists
  • Analytical Chemists, Microbiologists
  • QC/QA Professionals
  • Manufacturing Liaisons
  • Packaging Liaisons
  • Research & Product Development Scientists and Managers
  • Regulatory Affairs Personnel
  • Calibration and Validation Specialists
  • Facilities/HVAC Staff
  • Pharmaceutical Consultants

Course Description
This course focuses on the non-testing operational aspects of the stability function as practiced by the pharmaceutical, biological and medical device industries.

Establishing and maintaining strong stability operations programs will be covered, including: SOPs, training, protocols, life cycle stability strategies, storage conditions, chamber maintenance and monitoring, trending data and sample management.

Preparing for inspections and auditing of the stability function will also be covered. Considerable attention will be given to risk management as applied to all aspects of Stability Operations.

The impact of several stability guidances (ICH, WHO, and FDA, among others) on Stability Operations will be discussed. The course concludes with a workshop for hands-on experience in risk management and auditing of Stability Operations programs.
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   John O’Neill; Editor, stabilityhub.com

John O’Neill earned his Bachelor’s degree in Pharmaceutical Sciences from Columbia University and a Master’s in Health Systems Management from Union University. His career of 43 years has taken him from Registered Pharmacist to-Liquids and Semi-solids Formulator at Sterling Winthrop, QC Manager at Sanofi-Aventis, Medical Device Quality Steward at Boston Scientific, Independent Consultant, Principal Stability Specialist for Biologics at Genentech, and Associate Director for Stability at both Gilead and Regeneron. Mr. O’Neill currently serves as Stability Information Specialist for Nagano Science USA. He is a past chair of the Stability Working Group of the International Pharmaceutical Federation and is a member of the Product Quality Research Institute Stability Working Group for Shelf Life. Mr. O’Neill is a frequent conference speaker on stability topics. For the past 29 years he has been the Facilitator of the Pharmaceutical Stability Discussion Group, which has made him privy to just about everything that can go wrong or right with the Stability function.

Past participants in Mr. O’Neill’s industry programs have reported that he is knowledgeable, engaging, and a great story teller; bringing practical information backed by real-life experiences.
 
Deadline for Abstracts: N/A
 
Registration: Please click here for registration information.
E-mail: Jmorbit@cfpa.com
 
 
   
 
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