Expectations of Regulatory & Validation Master Planning - 2017

  • Check with publisher
  • Published date: May 15, 2017
    • Fremont, California, United States

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

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.

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

Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501353LIVE?channel=marketplace_Jul_2017_SEO

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