Toronto, Canada (PRWEB) October 30, 2012
The globalization of clinical trials presents challenges to all those involved in clinical trial, regardless of location. The role of the Qualified Person is essential in ensuring the smooth release of IMP in accordance with regulatory guidelines such as the EU Directive.
Xtalks presents an exciting new webinar which will discuss recent changes in regulatory requirements and their impact on the clinical supply chain, including:
Speaker Ronnie Constable, Director of Quality at Fisher Clinical Services will address these challenges as well as new approaches towards understanding and interpreting new regulatory requirements.
For more information about this event or to register, visit: http://xtks.in/-537p
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
To learn more about Xtalks visit http://xtalks.com/ContactUs.ashx
Karen Lim (416) 977-6555 ext 227