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:
Clinical and Manufacturing Staff
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
Compliance4All DBA NetZealous,