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How Ensuring Data Integrity in Method Validations

Event Details

How Ensuring Data Integrity in Method Validations

Time: February 28, 2018 from 10am to 11am
Location: Online
Street: 161 Mission Falls Lane, Suite 216,
City/Town: Fremont
Website or Map: http://www.compliance4all.com…
Phone: Event Manager
Event Type: online
Organized By: Adam Fleaming
Latest Activity: Dec 5, 2017

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Event Description

Overview:
The webinar will also illustrate the lifecycle management of analytical
procedures and train attendees on documentation requirements to
ensure Data Integrity.

Why should you Attend:
The guidance changes how FDA regulated methods will be developed,
validated and used. Additionally, how to ensure Data Integrity will be
discussed. The webinar will focus on detailing all key components of
the guidance and analyze its validation parameters, tests, and
acceptance criteria with respect to Data Integrity.

Areas Covered in the Session:
Scope and Content of the Guidance
Performing Pre-Validation Studies
Analytical Method Transfer Studies
Data Integrity and Documentation Requirements

Who Will Benefit:
Contract Laboratory Staff
Laboratory Managers and Staff
Analysts
QA Managers and Personnel
Regulatory Affairs Personnel

Speaker Profile:
Gary Miller has over 20 years in the R&D and manufacturing areas in
the pharmaceutical industry. Gary’s hands-on experience includes
investigations (product and manufacturing), product development,
manufacturing, quality, auditing, regulatory, project management, and
laboratory management.

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

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

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