{"href":"http://player.captivate.fm/services/oembed?url=http%3A%2F%2Fplayer.captivate.fm%2Fepisode%2F693857a8-f57b-421a-a6da-4f32c7047eda","version":"1.0","provider_name":"Captivate.FM","provider_url":"https://www.captivate.fm","width":600,"height":200,"type":"rich","html":"<iframe style=\"width: 100%; height: 200px;\" title=\"What is Regulatory Due Diligence for Medical Devices?\" frameborder=\"0\" scrolling=\"no\" allow=\"clipboard-write\" seamless src=\"http://player.captivate.fm/episode/693857a8-f57b-421a-a6da-4f32c7047eda\"></iframe>","title":"What is Regulatory Due Diligence for Medical Devices?","description":"What is regulatory due diligence? Why does it matter, and how does it differ from other regulatory strategies and pathways? \nIn this episode of the Global Medical Device Podcast, Jon Speer talks to Mike Drues of Vascular Sciences about the importance of and reasons for regulatory due diligence that all medical device professionals should understand.\nSome of the highlights of the show include:\n\u2022  Regulatory due diligence involves looking at what\u2019s been done so far when a company is developing a medical device similar to one on the market already.\n\u2022  Due diligence is important for business, regulatory, and engineering/product development perspectives to know before investing time, effort, and resources.\n\u2022  Differences and Similarities: Regulatory due diligence, regulatory strategy, and regulatory pathway to market are not synonymous and may depend on another. \n\u2022  Regulatory due diligence can be applicable to new or existing medical devices. Due diligence from an existing device provides essential background information.\n\u2022  Reminders/Requirements: Update regulatory due diligence in quality management system (QMS) and risk management plan through product lifecycle. \n\u2022  Past, Present, Future Challenges: Evolve and emphasize changes/corrections for prevention, design, risk, manufacturing, and regulatory perspectives.\n\u2022  Decouple and Rebuild: FDA is inherently concerned about entirely new and/or novel medical devices and technologies. \n\u2022  Take a cross-functional team approach to understand different perspectives, roles, and tasks to produce improved quality and regulatory due diligence.","thumbnail_width":300,"thumbnail_height":300,"thumbnail_url":"https://artwork.captivate.fm/d800dd76-19f4-4142-b90e-81a3b3899ef3/814a4686-7f39-4dcd-913f-4946e8d2fa4c.jpg"}