Healthcare Training by Compliance4all on FDA and Regulatory Aspects

Expired
Dates : 06 dezembro 2016 » 06 dezembro 2016

Place : Online Event
Estados Unidos

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Organizer :

Topic : Educação e ensino; Regulatory and Compliance Training
Ciências da Engenharia;
Keywords: Design, Manufacturing
Description :

Overview:  

This course explores some of the best practices of pharmaceutical facility design with an emphasis on regulatory aspects. FDA and other global regulatory body requirements are discussed and the reasoning behind them.

Examples of floorplans and flows (people, product, etc.) are examined and discussed. Specifics for fixtures, finishes, HVAC and other design aspects of cleanrooms are discussed in terms of current practices and GMP requirements. Examples of design choices for pressurization, flows and HVAC zones are given along with their possible application. Design specifications for both open and closed systems are discussed along with current standards. 

Why should you Attend: 

The attendee will learn what is important in facility design from the FDA and regulatory standpoint. The attendee will understand what FDA looks for during a facility inspection. The attendee will be able to minimize possible design errors which are difficult and expensive to fix post-build. The attendee will understand what FDA looks for in reviewing the facility design and the flow patterns.

Areas Covered in the Session:

Best design practices for Pharma facilities

Best design practices for biologics facilities

Regulatory compliance for Pharma and biologics facilities design

Flow patterns and cross contamination controls

Design criteria for fixtures and finishes

Examples of good design

General specifications for different classification zones

Examples of design specs for cleanrooms

Who Will Benefit:

Compliance Manager

Facility Manager

Validation Manager

Regulatory Manager

Design Team/Architects

Speaker Profile:

John R. Godshalk currently works for the Biologics Consulting Group as a Senior Consultant. John served as a Senior Review Biochemical Engineer and Lead cGMP inspector in the Division of Manufacturing and Product Quality at CBER, FDA. He contributed to formulation of FDA policy.

 

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com

http://www.compliance4all.com/

Event Link : http://www.compliance4all.com/control/w_product/~product_id=500884LIVE?channel=mailer&camp=webinar&AdGroup=sciencedz_Dec_2016_SEO

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Healthcare Training by Compliance4all on FDA and Regulatory Aspects to be held from 06 dezembro 2016 to 06 dezembro 2016 in Online Event, Estados Unidos. It covers various areas of Educação e ensino including Regulatory and Compliance Training. For more information, visit the website of the conference or contact the organizer.
Add to calendar 2016-12-06 2016-12-06 Europe/London Healthcare Training by Compliance4all on FDA and Regulatory Aspects https://www.sciencedz.net/pt/conference/23019-healthcare-training-by-compliance4all-on-fda-and-regulatory-aspects Online Event - Estados Unidos

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