Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies

Learn more about FDA’s current audit techniques and the most commonly cited GMP deficiencies that you have to watch out for. The webinar instructor, an FDA and GMP training expert, will help attendees analyze a system of risk assessments to determine audit frequencies.

Why Should You Attend:

The success of an audit by federal regulators does not always depend on the level of training proffered to staff and department employees, but also in understanding the focus of recent inspections within the industry. Such information provides a template for companies to analyze their own practices and ensure similar issues have been adequately addressed. In addition, as the audit techniques of the FDA have changed over the years, knowing what to expect can help establish a focused training program as part of the preparation.
This webinar will look at changes in FDA’s approach to audits and the current method used to determine audit frequencies by using a system of risk assessments.
Within the industries of pharma, biotechnology and medical devices, the word ‘audit’ can cause anxiety when you are unaware of how your company’s practices and procedures compare to the rest of the industry. Part of successfully getting through a regulatory audit involves: knowing the applicable regulations, the audit approaches used by regulators, and the common areas of industry deficiencies.

For Registration - http://www.complianceonline.com/current-fda-audit-practices-and-most-cited-gmp-deficiencies-webinar-training-703635-prdw?channel=worldconferencecalendar

Note: Use coupon code 232082 and get 10% off on registration.