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

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Category Software Staff, Clinical and Manufacturing Staff, Medical Laboratory

Deadline: January 21, 2019 | Date: January 23, 2019

Venue/Country: Online, U.S.A

Updated: 2018-11-07 15:11:10 (GMT+9)

Call For Papers - CFP

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

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.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com