This is a past event.

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

When: Tue., Aug. 13, 10-11:30 a.m. 2019
Phone: 8004479407
Email: compliance4all14@gmail.com
Price: 150.00
www.compliance4all.com/control/w_product/~product_id=502630LIVE?channel=clevescene_Aug_2019_SEO
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

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