FREE ON-DEMAND WEBINAR: JUNE 16, 2022

Bridging The Gap Between Development And Regulatory Teams

The mandatory nature of a regulatory-enabled process and the practical considerations of product design often create an undesirable tension between regulatory and development groups. 

The regulatory discipline needs a clear evolution of design inputs to design outputs with evidence and substantial justification. While developers may be prone to iterative solutions, which in turn, expose additional, nuanced needs. The intersection of these native tendencies creates a tension that can be counterproductive and obstructive to medical device development if not addressed. 

Register for this free, in-depth webinar presented by medical device expert Milton Yarberry, Director of Medical Programs at Integrated Computer Solutions, who will attempt a frank depiction of this collision of work practices, and focus on remedies in the form of processes, tools and approaches, that bridge the gap between development and regulatory.