Hardware Podcasts
Global Medical Device Podcast podcast cover art

Global Medical Device Podcast in 2021

66 episodes, newest first.

  1. 16 DecShaking Things Up: What's Next for the Global Medical Device Podcast34m
  2. 9 DecHow Augmented Reality (AR) is Revolutionizing Healthcare25m
  3. 2 DecWhy FDA is Prioritizing Clinical Decision Support Software & Why You Should Care31m
  4. 24 NovWhy Usability Matters25m
  5. 17 NovA Special Glimpse into Medtronic's Recent Developments in Spine & Biologics Technology17m
  6. 10 NovWhat are the Top Compliance Issues Plaguing Medical Device Manufacturers?30m
  7. 3 NovSetting the Record Straight on Usability & Human Factors36m
  8. 27 OctProject Management for Product Development of Medical Devices36m
  9. 21 OctAssessing the Global Regulatory Landscape24m
  10. 6 OctWhen to Throw the Least Burdensome Flag on FDA34m
  11. 22 SeptPast, Present, Future State (and World) of Quality in the Medical Device Industry27m
  12. 16 SeptFocusing on the Intent of the UDI Requirements from FDA's Final Guidance Doc38m
  13. 8 SeptAddressing the 'Who, What, When' of Quality in the Medical Device Industry28m
  14. 2 SeptMeet a Guru: Maryann Mitchell15m
  15. 25 AugWhy Storytelling Matters for Medical Device Companies26m
  16. 19 AugA Breakthrough Device that Aims to Prevent Osteoporosis24m
  17. 11 AugUnderstanding FDA's New Intended Use Rule and its Implications35m
  18. 28 JuleQMS in Academia: Practical Learning for Biomedical Engineering Students36m
  19. 19 JulTips for Running Better Management Reviews24m
  20. 14 JulMeet a Guru: Ryan Behringer27m
  21. 13 JulNavigating the MedTech Cybersecurity Ecosystem31m
  22. 7 JulManaging Clinical Data Activities24m
  23. 1 JulExplaining the Role of Importer under EU MDR34m
  24. 23 JunPreparing Your Pre-Submission with the Content FDA Wants to See36m
  25. 21 JunHow RADx Tech II Program is Fast-Tracking COVID-19 Technologies to Market in 202127m
  26. 16 JunHow New Training Partnership is Advancing Medical Device Knowledge & Professional Development15m
  27. 14 JunTop 3 Most Cited Issues in Medical Device Inspections from FDA FY202034m
  28. 9 JunHow Mindset Training Can Help Your Team Operate at Peak Performance28m
  29. 7 JunExamining the HHS Proposal for Premarket Notification Exemptions37m
  30. 2 JunCrash Course on Greenlight Guru Academy: How Medical Device Professionals Stay Ahead31m
  31. 31 MayBuilding your Brand as a Medical Device Professional37m
  32. 26 MayUnderstanding the Value of a Medical Device Guru32m
  33. 24 MayMeet a Guru: Etienne Nichols30m
  34. 19 MayMeet a Guru: Laura Court28m
  35. 17 MayRegulatory Tips & Pointers from a Former FDA Reviewer47m
  36. 12 MayWhy Demand is so High for Regulatory & Quality Jobs (and should you take advantage?)31m
  37. 11 MayComparing FDA’s Breakthrough Devices Program & Safer Technologies Program41m
  38. 7 MayWhy is IVDR Causing Widespread Panic throughout the Medical Device Industry?38m
  39. 3 MayManaging Business Risk as a Medical Device Company34m
  40. 28 AprWaterfall vs. Agile: Battle of the Product Development Methodologies38m
  41. 26 AprFor the Love of Internal Auditing33m
  42. 21 AprSimilarities & Differences between In Vitro Diagnostic (IVD) Devices & Medical Devices34m
  43. 19 AprKnowing vs. Doing as Medical Device Professionals31m
  44. 14 AprPivoting Operations to Meet PPE Demand during Pandemic27m
  45. 13 AprPros & Cons of Being a Physician turned MedTech Inventor49m
  46. 7 Apr3 Systems of Risk for Medical Devices from FDA39m
  47. 5 AprQuality Management for IVD Devices vs Medical Devices41m
  48. 31 MarUnderstanding the Investigational Device Exemption (IDE) Process57m
  49. 30 MarEvaluating, Monitoring & Selecting Suppliers in the Medical Device Industry22m
  50. 25 MarWhy the PMA Process is so Dreaded by Manufacturers in the US Market46m
  51. 24 MarLearning about the Real-world Impact of Design, Manufacturing, Quality & Culture on Patients37m
  52. 21 MarWhat is the Safer Technologies Program (STeP) and Can Your Device Use It?32m
  53. 17 MarMeet a Guru: Sara Adams20m
  54. 10 MarBuilding a Startup in the MedTech Industry30m
  55. 8 MarMeet a Guru: Karen Schuyler25m
  56. 4 MarVisualizing a Medical Device through Illustrations, Animations, and other Artwork43m
  57. 1 MarEverything you Need to Know about SaMD from an FDA Perspective46m
  58. 24 FebPreparing for Remote and On-Site Inspections and Audits50m
  59. 22 FebHow does EU MDR impact your Quality Management System?36m
  60. 18 FebVirtual Auditing in a Post-COVID World of Digital Compliance30m
  61. 10 FebInside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View40m
  62. 4 FebPrioritizing Medical Device Reimbursement During Product Development40m
  63. 27 Jan5 Actionable Lessons Learned from the RADx Initiative by NIH47m
  64. 20 JanWhat are the Strategic Priorities for CDRH in 2021?46m
  65. 14 JanUnderstanding and Handling Different Types of Feedback34m
  66. 7 JanMeasuring the Impact of AI/ML Technologies on the Current Medical Device Landscape44m