What Good Documentation Practices [Experts] Don't Want You To Know

  • 150.00 Dollar US$
  • Published date: November 13, 2018
    • Fremont, California, United States

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:
Material or product identity, quality, purity, strength and safety
The validated state of GMP /GLP /GCP product manufacture, facilities, equipment, computer systems and testing methods

Areas Covered in the Session:
Basics of Good Documentation Practices
Documents vs records
How to write or record information in a compliant way
How to amend documents or records in a compliant way

Who Will Benefit:
Laboratory
Clinical and Manufacturing Staff
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. Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Microbiology, Food Safety & Turnarounds.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com

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Compliance4All
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