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How Ensuring Data Integrity in Method Validations

 
  December 05, 2017  
     
 
Netzealous LLC DBA - Compliance4All, Online
2018-02-28


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

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
 
 
Organized by: Event Manager
Invited Speakers:
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.
 
Deadline for Abstracts: 2018-02-27
 
Registration:

Full Details & Registration Link:

http://www.compliance4all.com/control/w_product/~product_id=501679LIVE?channel=molgen_Feb_2018_SEO 

E-mail: support@compliance4All.com
 
   
 
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