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Expectations of Regulatory & Validation Master Planning - 2017

 
  May 12, 2017  
     
 
Netzealous LLC DBA - Compliance4All, Online
2017-07-20


Overview:  
This presentation will cover the importance of master planning. The FDA and other regulatory bodies expect these to be among the Quality System documentation.

Areas Covered in the Session:
History and background
Types
Organization
Requirements
Regulatory expectations
Maintenance

Who Will Benefit:
Compliance Personnel
QA Personnel
validation Personnel

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
 
 
Organized by: Event Manager
Invited Speakers:
Speaker Profile: 
Louis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of experience in Quality Assurance, Quality Control, Validation, consent decree remediation as well as cGMP Compliance in the Medical Device and Pharmaceutical industries.
 
Deadline for Abstracts: 2017-07-21
 
Registration:

Full Details & Registration Link:

http://www.compliance4all.com/control/w_product/~product_id=501357LIVE?channel=hum-molgen_Jul_2017_SEO 

E-mail: support@compliance4All.com
 
   
 
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