Netzealous LLC DBA - Compliance4All, Online
2019-01-23
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
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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