2019 - The GxP Audit Report and The Savannah Brain
Date2019-12-03
Deadline2019-12-02
VenueFremont, USA - United States
KeywordsCompliance trainings; Savannah Brain; Compliance Standards
Topics/Call fo Papers
Overview:
This 90 minute webinar focuses on three critical areas of audit report writing:
content, presentation and readers.
Why should you Attend:
A well-written audit report is a call to action and a rich source of process and
product quality data. How an audit report is written can make all the difference in
how facts and recommendations are received.
Areas Covered in the Session:
Interpretive Writing
Format & Length
Style, Design & Tone
Grammar and Syntax
Plague Words & Phrases
Who Will Benefit:
Process Owners
QA, QC and Continuous Improvement Managers & Staff
Regulatory and Compliance Managers
Change Control
Speaker Profile:
William D Fox is a quality management professional with a background in clinical
research and quality assurance. William’s experience includes scientific,
administrative, and quality aspects of regulated (ISO, GCP, GLP, GMP)
pharmaceutical development and manufacturing and spans the translational
interface.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14-AT-gmail.com
This 90 minute webinar focuses on three critical areas of audit report writing:
content, presentation and readers.
Why should you Attend:
A well-written audit report is a call to action and a rich source of process and
product quality data. How an audit report is written can make all the difference in
how facts and recommendations are received.
Areas Covered in the Session:
Interpretive Writing
Format & Length
Style, Design & Tone
Grammar and Syntax
Plague Words & Phrases
Who Will Benefit:
Process Owners
QA, QC and Continuous Improvement Managers & Staff
Regulatory and Compliance Managers
Change Control
Speaker Profile:
William D Fox is a quality management professional with a background in clinical
research and quality assurance. William’s experience includes scientific,
administrative, and quality aspects of regulated (ISO, GCP, GLP, GMP)
pharmaceutical development and manufacturing and spans the translational
interface.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14-AT-gmail.com
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Last modified: 2019-11-11 14:07:35