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

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: [email protected]