How FDA Trains its Investigators to Review CAPA - 2017
- Start Date:
- Monday, 15 May, 2017
- End Date:
- Monday, 15 May, 2017 11:00am
- Business Practice, Health & Nutrition
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 InspectorsInvestigations Operations Manual (IOM)CPG Manual 7382.845QSIT ManualWho Will Benefit:QA managementCAPA coordinatorRegulatory Affairs managementExecutive managementSpeaker 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.Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: support@compliance4All.com
161 Mission Falls Lane,
Conference organized by Compliance4ALL
Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. .Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.
- 161 Mission Falls Lane, Suite 216