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32801 Conferences

A Comparison of ICH Q-10 Quality System and the FDA's Quality Systems Approach (QSA) to the Pharmaceutical GMPs - Webinar By GlobalCompliancePanel

Added by davidross759 on 2010-11-24

Conference Dates:

Start Date Start Date: 2011-01-11
Last Date Last Day: 2011-01-11

Conference Contact Info:

Contact Person Contact Person: Webinars
Email Email: webinars@globalcompliancepanel.com
Address Address: Online Training, Wilmington, DE, 19801, United States
Phone Tel: 800-447-9407
Phone Fax: 302-288-6884

Conference Description:

Overview: In September of 2006, the FDA published the Quality System Approach to Pharmaceutical Good Manufacturing Practices which provided a quality orientation to the GMP's

Then in June of 2008, The International Conference on Harmonization (ICH) published ICH-Q10, Pharmaceutical Quality System. These guidance documents have provoked thought and raised questions about existing pharmaceutical.

During this webinar, the present status of these Guidances will be discussed and suggestions for their implementation will be presented. This webinar will be very informative for Quality Assurance personnel who have the desire to move toward implementing quality concepts rather than focusing on the strict rules of compliance. This webinar will show how to strike a balance between compliance and quality.

Areas Covered In the Session:

* What are the objectives of ICH-Q10 and the FDA's Quality Systems Approach to Pharmaceutical Good Manufacturing Practices?
* What are the similarities and differences between these guidance documents?
* What are some Pro and Cons of the product lifecycle for pharmaceuticals
* Is the Quality Systems Approach really "Compliance in Sheep's Clothing?
* Who will win the GMP battle-Quality or Compliance

Who Will Benefit:

* Quality Unit Supervisors/Managers/Directors
* Manufacturing Supervisors/Managers/Directors
* Support Functions to Quality or Manufacturing
* Regulatory Affairs personnel responsible for GMP Compliance and filings
* Support personnel responsible for GMP Related activities such as Calibration and Testing Functions
* Validation personnel
* R&D Professional, Supervision and Management
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