FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies

Website http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500239?expDate=Ourglocal | Edit Freely

Category seminar; webinar; Pre Market Application,510(k),quality system,new diagnostic assay,Good Laboratory Practices and Good Manufacturing Practices, travel and entertainment,reimbursement fraud,reimbursement fraud,Anti-Fraud Control,exploit weaknesses, Banking and Financial act, Backstabbers, Communication, Gossip, Insecurity, Leading, Marks of leaders, Personal Growth, Taking others higher, health; medical; pharma; clinical; drug;

Deadline: April 29, 2014 | Date: April 29, 2014

Venue/Country: 38868 Salmon Ter, Fremont, California, U.S.A

Updated: 2014-03-17 21:15:16 (GMT+9)

Call For Papers - CFP

Description:

In preparing for a regulatory audit, two very important sources of information to seek include knowing what the auditors will look for as areas of focus and what have been the most commonly cited drug GMP deficiencies. These items will help companies to better evaluate their own practices, address similar deficiencies that may have been found during internal audits and to prioritize their efforts so as to make sure they do not become another statistic of the top 10 most drug cited GMP deficiencies for 2012-2013.

Why Should you Attend:

By knowing the audit techniques and current areas of focus used by auditors, this webinar will help companies in their preparation and training of applicable personnel as to how best to get through the audit. The most common cited GMP deficiencies for drugs will be reviewed to provide a template against which companies can evaluate their own state of compliance and to correct those areas where similar deficiencies are noted. Preparation is the key to passing any audit and the information to be discussed in this webinar is an excellent resource to use.

Objectives of the Presentation:

This webinar will provide attendees an overview of current audit approaches used by regulatory inspectors and the opportunity to see what has been the most commonly cited GMP deficiencies. This information can be used as a training tool for such audits and a template for helping to assure a state of compliance.

Who can Benefit:

Production

Quality Assurance

Quality Control

Regulatory

Vendors

Engineering

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