The Medical Devices Group

03 FDA Strategies to Avoid Stunning Disaster

1 h 52 min · 20. okt. 2019
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Beskrivelse

Regulatory expert Rob Packard has seen brilliant medtech companies blow up for stupid – and easily avoidable – errors. I hope you’ll invest time to hear what he has to say about FDA submissions – especially De Novos that require clinical testing. In this episode, Rob offers practical strategies to help you conserve cash, test smarter, and be better prepared for your all-important FDA submission. For the video replay and slides, see https://medgroup.biz/dnovo [https://medgroup.biz/dnovo]. This episode is sponsored by Tommy, Alan, and Ross Cooper at CooperConsultingService.com [https://CooperConsultingService.com].

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The first of our weekly calls to see how we can mobilize our Medical Devices Grou [https://MedicalDevicesGroup.net]p (350,000+ members) to expedite a solution to the COVID-19 pandemic. Join our next call at https://medgroup.biz/cvd19 [https://medgroup.biz/cvd19]; our chatroom at https://medgroup.biz/cvslk [https://medgroup.biz/cvslk]. Both are free to subscribers. Our panelists were: Daniel Kraft, MD [https://www.linkedin.com/in/dkraft/] (Singularity University) Celine Teoh [https://www.linkedin.com/in/celineteoh/] (Headland Strategy)  Mark Michalski [https://linkedin.com/in/mark-michalski-b3b23411/] (Headland Strategy)  Scott Herskovitz [https://linkedin.com/in/scott-herskovitz-711228/] (Qosina Medical Supply)  George Friou [https://www.linkedin.com/in/george-friou-2ab9b015/] (Josephine Caring Community)

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