Regulatory Affairs for Medical Device Clinical Trials with Priya Jagasia

<p><span style="font-weight: 400;">Clinical trials are conducted in compliance with regulations. </span></p> <p><span style="font-weight: 400;">Simply stated, you need a clinical and regulatory strategy when it comes to conduct of clinical trials for medical devices.</span></p> <p><span style="font-weight: 400;">As a clinical researcher, there have been times I’ve felt lost because I did not understand the regulatory framework.</span></p> <p><span style="font-weight: 400;">To close this knowledge gap, I thought it would be great to invite Priya Jagasia, Divisional Vice President (DVP) of Regulatory Affairs at Abbott Vascular on the show.</span></p> <p><span style="font-weight: 400;">In this episode, Priya shares with us her experience and knowledge on regulatory affairs, specifically focused around medical device regulations in the United States.</span></p> <p><span style="font-weight: 400;">She does a great job of tailoring our conversation to make it applicable for clinical trial professionals.</span></p> <p><span style="font-weight: 400;">We cover topics such as working with the FDA, partnership between regulatory affairs and clinical research, career and professional development, and much more.</span></p> <p><span style="font-weight: 400;">The art and science of regulatory affairs is fascinating and there is no better person on the planet who can educate us on this topic.</span></p> <p><span style="font-weight: 400;">Please join me in welcoming Priya Jagasia on the Clinical Trial Podcast.</span></p> <p><span style="font-weight: 400;"><strong>Podcast Sponsor:</strong> This episode is brought to you by Florence Healthcare. To learn more, visit</span> <a href= "https://florencehc.com/"><span style= "font-weight: 400;">florencehc.com</span></a></p>