Expectations of Regulatory & Validation Master Planning – 2017

Start Date : July 20, 2017
End Date : July 20, 2017
Time : 10:00 am to11:00 am

Phone : (800) 447-9407
Email : support@compliance4All.com

Description

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

Organized by

Organized by compliance4all14

Compliance4ALL ,
161 Mission Falls Lane, Suite 216,

Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. .

Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.

Tel: 18004479407
Email: support@compliance4All.com
Website: http://www.compliance4all.com


Event Categories: Health & Nutrition.

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