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Ready to move into the MDR space? This podcast is for you, if you’re facing challenges within all stages of getting a product to market. To help you we’ve gathered...
show more
Ready to move into the MDR space?
This podcast is for you, if you’re facing challenges within all stages of getting a product to market. To help you we’ve gathered some of the greatest and most influential minds in the Medical Device industry, to get their insights on how to go from an idea to a market success.
You'll be accompanied by our host, Helene Quie, the founder and CEO of Qmed Consulting.
show less
This podcast is for you, if you’re facing challenges within all stages of getting a product to market. To help you we’ve gathered some of the greatest and most influential minds in the Medical Device industry, to get their insights on how to go from an idea to a market success.
You'll be accompanied by our host, Helene Quie, the founder and CEO of Qmed Consulting.
23 OCT 2024
8 FEB 2024 · During this episode we will have CETAS Healthcare share their extensive knowhow and perspective on how to set up PMCF surveys and gather important data fulfilling the MDR requirement.
13 JAN 2024 · Ted Heise from the MedInstitute is a true subject matter expert within biocompatibility and biological evaluation. He will share during this interesting conversation his view on how to understand the guidances and regulations in the key markets.
1 DEC 2023 · I am thrilled to host Rikke Bøge, an esteemed Clinical Affairs Subject Matter Expert, as our special guest on this episode of the Qmed podcast. Rikke's extensive background as a nurse, study coordinator, and Clinical Research Associate brings a depth of experience that's invaluable. She will be sharing her wealth of knowledge and firsthand experiences during audits in the clinical research landscape.
Tune in as we explore real-life scenarios, insights, and strategies to navigate the intricacies of audits in clinical settings. Don't miss this opportunity to gain valuable insights from Rikke's expertise!
3 NOV 2023 · During this episode I speak with the subject matter expert Dr. Susanne Gerbl-Reiger about the implementation of MDR and ISO14155 and typical findings observed during her long time experience form AKRA team and TÜV SÜD
29 SEP 2023 · In this third episode of the Qmed Podcast we discuss the process of identifying, analysing and consluding on the Risk Benefit Assessment. I am interviewing David Rudledge who shares his experience and knowledge working within this field for medical devices the last 25 years. Listen and enjoy!
15 MAR 2023 · Have you ever wondered how digital health is driving the future of healthcare?
Don't miss our new podcast on "Digital Health And Reimbursement" where Ernesto Nogueira and Helene Quie explore the impact of COVID-19 on digital medical technologies, the different types of digital health, and their applications in healthcare.
Ready to move into the MDR space? This podcast is for you, if you’re facing challenges within all stages of getting a product to market. To help you we’ve gathered...
show more
Ready to move into the MDR space?
This podcast is for you, if you’re facing challenges within all stages of getting a product to market. To help you we’ve gathered some of the greatest and most influential minds in the Medical Device industry, to get their insights on how to go from an idea to a market success.
You'll be accompanied by our host, Helene Quie, the founder and CEO of Qmed Consulting.
show less
This podcast is for you, if you’re facing challenges within all stages of getting a product to market. To help you we’ve gathered some of the greatest and most influential minds in the Medical Device industry, to get their insights on how to go from an idea to a market success.
You'll be accompanied by our host, Helene Quie, the founder and CEO of Qmed Consulting.
Information
| Author | Qmed Consulting |
| Organization | Qmed Consulting |
| Categories | Health & Fitness , Medicine |
| Website | www.qmed-consulting.com |
| qmedpodcast@gmail.com |
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