Validation Master Plans, Batch Requirements Among New Session Topics
(Chicago, IL) – The most popular event for validation professionals in the medical device and diagnostic space is back with presenters from leading companies and new topics on the agenda. The 2nd Annual Medical Device and Diagnostic Process Validation Conference will be held July 20-21, 2015 in Arlington, Virginia, offering a wide variety of networking and idea sharing opportunities with implementable takeaways.
This year, topics will address a plethora of challenges that validation professionals currently face, including reducing time-to-market, new regulatory requirements, risk assessment, and more. Some of the most influential and successful leaders within the validation space will be on hand to lead sessions, panel discussions, and case studies, including Sreya Chatterjee of Stryker, Darric Inselman of Depuy Synthes, and Kamalesh Saha of Medtronic. Sessions will include an open-floor format with time for question-and-answer and further discussion.
The conference will offer exclusive FDA insight on several topics, such as inspection trends for validation procedures, test method validation, and reusable medical devices. Conference delegates will take away new ideas, in-depth perspectives and information, and strategies for remaining competitive in the changing validation landscape.
For more information on the 2nd Annual Medical Device and Diagnostic Process Validation Conference, please contact marketing@q1productions.com. You can also follow the conference on Twitter @Q1Productions.
