FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries July 26, 2012

Understanding GLP regulations and requirement and achieving GLP compliance can significantly expedite the regulatory processes, bringing innovative medical products to the market faster and saving enormous amount of your unnecessary time, efforts and investment.

During this interactive workshop, Dr. David Lim (Regulatory Doctor) will walk you through the relevant and applicable US regulations, regulatory requirements and guidance necessary for good laboratory practice (GLP) and GLP compliance. This workshop is intended to provide guidance on GLPs for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for pharmaceutical and medical device products for human use regulated by the United States Food and Drug Administration (US FDA). During this workshop (2nd day), group discussions on implementing GLPs will be engaged.

Official Website: http://www.complianceonline.com/ecommerce/control/seminar?product_id=80036SEM&?channel=yahooevent