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FDA’s Current Good Tissue Practice Regulations: An Introduction

  
  April 14, 2016
Pharma Development and Business
  
     
 
CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
May 17, 2016 at 11:00 a.m.–12:30 p.m. (ET)

Who Should Attend?
This online training course will benefit professionals in the following industries: Human Cellular Therapies, Tissue Therapies, and Human Cell and Tissue-based Products (HCT/Ps).

This online training course will be of benefit to all persons whose span of responsibility includes compliance with the U.S. Food and Drug Administration’s (FDA’s) Current Good Tissue Practice Regulations (CGTPs) including, but not limited to scientists and other professionals in: Quality Assurance, Quality Control, Regulatory Affairs, Compliance, Development, Manufacturing and Production.

Course Description
This intensive 90-minute accredited online training course focuses on becoming proficient at knowing when and in what situations CGTP—and related—compliance is required for HCT/Ps. The overall approach is to turn theory into practice so you can put what you learn in this course to immediate use to assure your company’s CGTP activities, and those of any contract facilities, meet the regulatory and technical requirements and expectations of the US FDA. The course materials include comprehensive reference and resource lists to provide answers to compliance questions and guide your CGTP compliance efforts.

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: May 18, 2016
  
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
Thomas J Pritchett, Ph.D., Consultant

In his more than 25 years working with the US, European, Canadian and other pharmaceutical, biopharmaceutical, and biologics industries, Dr. Tom Pritchett has gained considerable experience in most aspects of Quality Assurance, Quality Control and CGTP and CGMP Compliance for both investigational and marketed products. He is also an experienced teacher, and has been directing courses for the Center for Professional Advancement since 1995. In addition, Dr. Pritchett has provided training sessions for the US FDA, for the US National Institutes of Health (NIH), and for officials, regulators, and industry professionals of countries in the Gulf Cooperation Council (GCC). Dr. Pritchett is also an industry consultant and the co-founder/publisher of the newsletter BioQuality (www.bioquality.biz).
 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
 
   
 
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