Complying with FDA's Good Documentation Practices [It Didn't Happen]

Event Details

  • DateTue 13 August 2019
  • Time10:00 AM - 11:30 AM
  • VenueOnline
  • Location161 Mission Falls Lane, Suite 216, Fremont National 9453
  • TypeWorkshop
  • Ticket$$150 per person
  • Table$Price for a table per table (seats Normally between 8-12)
  • ContactNetzealous LLC DBA - Compliance4all
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Overview: In a pharmaceutical or medical device environment documentation needs to meet certain requirements to ensure product quality and product safety. Why should you Attend: As the FDA and TGA say "If it isn't written down, then it didn't happen". To meet industry standards, it is critical that all documentation follows GDP when it affects: GMP /GLP /GCP processes Material or product identity, quality, purity, strength and safety Areas Covered in the Session: Document Approval Handwritten Entries Copies of Documents Document Maintenance Document Modification Warning Letters for GDocP Who Will Benefit: Anyone that creates records in a regulated industry including Laboratory, Clinical and Manufacturing Staff, as well as IT /Software Staff Speaker Profile: Angela Bazigos is the CEO of Touchstone Technologies Inc. She has degrees in Microbiology and Computing and 40 years of experience in the Life Sciences, Healthcare & Public Health Services. Event Fee: One Dial-in One Attendee Price: US $150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: