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

Date : 13th August 2019 to 13th August 2019

Place : United States, Fremont

Website :https://www.compliance4all.com/control/w_product/~product_id=502630LIVE?channel=allconferencealerts_Aug_2019_SEO

Contact Person:Event Manager

Description:

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 Who Will Benefit: Anyone that creates records in a regulated industry including Laboratory, Clinical and Manufacturing Staff, as well as IT /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. Event Fee: One Dial-in One Attendee Price: US $150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: [email protected]

Complying with FDA's Good Documentation Practices [It Didn't Happen] will be held in Fremont,United States on date 2019-08-13

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Deadline for abstracts/proposals : 11th August 2019

Keynote Speakers :

Venue :Fremont, CA, USA

Check the event website for more details.