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

 
  November 27, 2018  
     
 
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
 
 
Organized by: Event Manager
Invited Speakers:

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.
 
Deadline for Abstracts: 2019-01-22
 
Registration: https://www.compliance4all.com/control/w_product/~product_id=502246LIVE?channel=hum-molgen_Jan_2019_SEO
E-mail: compliance4all14@gmail.com
 
 
   
 
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