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How FDA Trains its Investigators to Review CAPA - 2017

 
  March 17, 2017  
     
 
Compliance4All, Online
2017-05-15


Overview:  
In this session will be a section-by-section summary of the CAPA subsection of the QSIT, the document by which FDA inspectors operate during an inspection, as well as how your company can use that same document to increase the likelihood of a positive outcome during the inspection.

Areas Covered in the Session:
Documents Used by FDA Inspectors
Investigations Operations Manual (IOM)
CPG Manual 7382.845
QSIT Manual

Who Will Benefit:
QA management
CAPA coordinator
Regulatory Affairs management
Executive management

Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
 
 
Organized by: Compliance4All
Invited Speakers:

Speaker Profile:
Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy and colonoscopy devices, where he oversees the operation of the quality system. In this position, Jeff is responsible for oversight of the document control system, including maintenance of regulatory documentation.
 
Deadline for Abstracts: 2017-05-14
 
Registration:

Full Details & Registration Link:

http://www.compliance4all.com/control/w_product/~product_id=501265LIVE?channel=mailer&camp=Webinar&AdGroup=hum-molgen_May_2017_SEO 

E-mail: support@compliance4All.com
 
   
 
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