A(z) Medical Device csatorna legjobb podcastjai (2024)

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#367: Interviewing the Interviewer 39:44

16h ago39:44

39:44

In this special episode of the Global Medical Device Podcast, Etienne Nichols switches roles from host to guest as Devon Campbell turns the tables to explore the invaluable lessons Etienne has learned from over 100 podcast episodes. Delve into key insights on product development, quality management, and the power of vulnerability and networking. Et…

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Are you more Corrections or Corrective Actions or Preventive Actions?

3d ago

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Do you have to manage complaints, CAPA, Non-conformances, audits, management reviews… for your company. Then you need to put in place actions. Today we will explain to you with Vincent Cafiso what are Correction, Corrective Actions and Preventive Actions. Who is Vincent Cafiso Named as one of MD+DI’s 24 Medtech Voices to Follow in 2024, Vincent Caf…

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A Day In The Life Of A Successful Female Medical Device Representative 1:00:30

3d ago1:00:30

1:00:30

In This Special Episode, I Will Be Joined By A Guest In The Name Of Courtney Turich, She Is Linked-In Top Sales Voice, Global VP Of Sales, And Marketing, Dynamic Leader, Change Agent And Strengths Champion. In 2014's Season 5, Episode 22 Of The Popular TV Show Shark Tank, She Landed A Deal And Ended Up Partnering With Mark Cuban and Lori Greiner An…

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Finance to Medical Device Sales in 5 Weeks with Chase Blum 25:34

7d ago25:34

25:34

Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medical-device-sales First Year in Ebook: https://www.newtomedicaldevicesales.com/prod…

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Commercializing a Disruptive Technology in a Hospital with Multiple Decision Makers and Influencers - Featuring Joe Steele 1:00:54

16d ago1:00:54

1:00:54

Joe Steele is Head of Commercialization at Hemosonics, where they are providing point-of-care solutions to help clinicians make more informed decisions on blood product usage. In this episode Joe shares why moving up the ladder too fast may not be the best way to go, why experiencing failure will help in the long-run, how to use wisdom from past ex…

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2024-07: Wie Sie dem Gesundheitswesen direkt helfen können 13:45

24d ago13:45

13:45

Ein wirklich nachhaltiges Projekt benötigt Ihre Spende alter Computer Bereits seit über zehn Jahren hilft der Verein HITA e.V. (Healtchare IT for Africa) Pflegekräften und Hebammen im Ghana bei der Weiterbildung, indem er Lernarbeitsplätze mit PCs ausstattet und am Laufen hält. Dabei spielt die Nachhaltigkeit eine große Rolle: Ausschließlich alte P…

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How to select and evaluate your Contract Manufacturer?

10d ago

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Medical Device manufacturers can also involve third party companies to manufacture their devices. We call them Contract Manufacturers. But they are only your supplier and not the legal manufacturer of the product. So now the question is how to select them and also how to handle them. Let’s find that out with Keith Smith from Vonco Who is Keith Smit…

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The Power Of Preparation 59:51

10d ago59:51

59:51

In The Fast-Paced And Ever-Evolving Field Of Medical Device Sales, Preparation Is Key. It's What sets apart The Top Performers From The Rest. Today, We'll Uncover The Strategies, Techniques, And Mindset Required To Excel In This Competitive Industry Through Effective Preparation. Join Your Host Gyda Loveres And Her Guest Jarett Mitchell, A Pharmace…

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It Is Never The Right Time In Medical Device Sales 22:39

13d ago22:39

22:39

Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medical-device-sales First Year in Ebook: https://www.newtomedicaldevicesales.com/prod…

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#366: Cardiac Arrest: Five Heart-Stopping Years as a CEO on the Feds Hit-List 55:39

15d ago55:39

55:39

In this episode of the Global Medical Device Podcast, host Etienne Nichols engages with Howard Root, former CEO of Vascular Solutions and author of "Cardiac Arrest: Five Heart-Stopping Years as a CEO on the Fed’s Hit List," and Mark Duval, President and CEO of DuVal & Associates. The episode delves into the harrowing experiences of navigating sever…

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Quality Field Service for Medical Devices

17d ago

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Michael Israel from Zuper.co is helping us understand the world of Field Service and then we can understand better how some information collected by Field Service Engineer can help Quality Department to have a better operation. Collect machine performance, train technicians, identify issues. Michael will also talk about Zuper which is a FSM softwar…

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Navigating The World Of Medical Device Sales 57:34

17d ago57:34

57:34

In This Very First Episode, Join Gyda and Her Special Guest Jeff As They Uncover The Secrets, Challenges, And Triumphs That Come With Selling Medical Devices. You Will Hear Firsthand Stories From Industry Professionals, Gain Insights From Experts, And Navigate Through The Unique Landscape Of This Dynamic Field. Throughout This Podcast, I Will Featu…

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Top Candidates Have Leverage In Medical Device Sales 17:27

21d ago17:27

17:27

Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medical-device-sales First Year in Ebook: https://www.newtomedicaldevicesales.com/prod…

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Medical Device NewsMAY 2024 Regulatory Update

21d ago

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EU Notified Bodies TUV SUD Denmark under MDR –Welcome to the Brother or Sister: https://api.tech.ec.europa.eu/nando-prod/files?repo=nando&id=150a0abbc0d4397086d648963fc940a321e02c11&group=NOTIFICATION&download=true AFNOR 46th NB under MDR –Finally a second one for France: https://webgate.ec.europa.eu/single-market-compliance-space/#/notified-bodies…

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#365: Medical Device Reporting: The Do's and Don'ts 40:55

21d ago40:55

40:55

In this episode, Lisa Van Ryn, a seasoned expert from Greenlight Guru, shares her extensive knowledge on the FDA’s Medical Device Reporting (MDR). We unpack the nuances of when and how to report incidents, the definition of serious injuries, and the importance of effective complaint management systems. Lisa provides practical advice on setting up r…

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#364: Building a Partnership with your Regulatory Consultant 40:02

24d ago40:02

40:02

In this episode, host Etienne Nichols speaks with Christine Luk, Associate Regulatory Affairs Manager at Proxima, about her journey through the medical device sector. From her academic beginnings in biochemistry and biomedical engineering to founding a startup and navigating FDA regulatory pathways, Christine offers a wealth of knowledge. The discu…

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Open or Closed Robotic Systems – Are We at a Crossroads? Featuring Stuart Simpson 1:04:38

23d ago1:04:38

1:04:38

Stuart Simpson is CEO of Think Surgical. During his stellar 24-year career at Stryker he led an orthopedic industry transformation that established surgical robotic joint replacement as a standard of care, beginning with the acquisition of Mako Surgical in 2013. In this episode he shares his roots in medical device and how orthopedics became his pa…

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How To Turn Calls Into Interviews In Medical Device Sales 26:05

28d ago26:05

26:05

May 4th Scottsdale Arizona Meetup: https://www.newtomedicaldevicesales.com/event Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medic…

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#363: Bringing a Self-Funded Medical Device to Market 39:12

29d ago39:12

39:12

In this insightful episode of the Global Medical Device Podcast, host Etienne Nichols delves into the journey of Dr. Lee Hunter, an orthopedic surgeon and innovator in elbow surgery devices. Dr. Hunter shares his experience from the conception of a simple yet effective surgical device through its development, struggles with initial licensing, and u…

1
#362: Managing Risk in Clinical Investigations 39:43

1M ago39:43

39:43

In this episode of the Global Medical Device Podcast, host Etienne Nichols engages with Helene Quie, an expert in medical device regulations and clinical investigations. They delve into the dual aspects of risk management: ensuring product safety and the procedural risks associated with clinical protocols. Helene emphasizes the importance of a meas…

1
Why and how to build a Quality Culture?

1M ago

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A quality culture seem to be a nice to have. But after listening this podcast episode with Lesley Worthington, you will see that it is worth to build one. We will review the description of a quality culture and how to build it. But also if this is required by a regulation and how you can align it with your compliance duties. Check this and share it…

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Veteren and Nurse Breaks into Medical Device Sales with Drew Stanly 34:15

1M ago34:15

34:15

May 4th Scottsdale Arizona Meetup: https://www.newtomedicaldevicesales.com/event Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medic…

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#361: Speaking the Language of IVD 44:21

1M ago44:21

44:21

In this episode of the Global Medical Device Podcast, host Etienne Nichols delves into the intricate world of in vitro diagnostics (IVDs) with Christie Hughes, a principal consultant and IVD expert at Qserve Group. With over 25 years of experience, Christie shares her extensive knowledge, discussing the nuances of IVDs, regulatory landscapes, and p…

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What is the impact of AI Act on Medical Devices?

1M ago

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The AI Act or Artificial Intelligence Act is now a reality. But what does it mean for the Medical Device industry and what should you do within your Quality or Regulatory affairs activities. Erik Vollebregt, from Axon Lawyers will tell us what we should understand with this new legislation and what are the consequences for the Medical Device commun…

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#360: Is It Possible to "Buy" a QMS? 32:27

1M ago32:27

32:27

In this episode of the Global Medical Device Podcast, Etienne Nichols engages with Sara Adams to discuss Quality Management Systems (QMS) in the medical device industry. The discussion unveils the complexities and common misconceptions surrounding QMS, drawing an intriguing analogy between building a QMS and crafting sourdough bread. Sara shares he…

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22 year old Breaks In Medical Device Sales in 2 Weeks with Joe Dobbs 38:06

1M ago38:06

38:06

May 4th Scottsdale Arizona Meetup: https://www.newtomedicaldevicesales.com/event Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medic…

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Radiation Sterilisation Master File (ISO 11137 & 11607)

1M ago

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If your products need to be sterilized, then you will need to prove that the sterilization process is validated and continues to work all through the life to the product. So Adam Isaacs Rae will provide you with the information on Radiation Sterilization requirements. Standards, guidelines, pitfalls. All this will help you remain compliant. Who is …

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2024-06: Rechtliche Anforderungen an Cloud-Lösungen (mit Prof. Strittmatter) 31:13

2M ago31:13

31:13

Was Medizinproduktehersteller (nicht nur) bei der Vertragsgestaltung beachten sollten Medizinproduktehersteller nutzen die Cloud für ihre internen IT-Systeme, zum Beispiel um ein ERP zu betreiben oder sogar mit einem cloudbasierten ERP zu arbeiten. Gleichzeitig nutzen einige Hersteller die Cloud, um selbst Dienstleistungen anzubieten, wie das beisp…

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Who You Listen To Matters with Jason Elmore 25:16

2M ago25:16

25:16

Web Page To Meetup: https://www.newtomedicaldevicesales.com/event Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medical-device-sales…

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#359: Project Management in MedTech 1:02:20

2M ago1:02:20

1:02:20

This episode of the Global Medical Device Podcast features a compelling conversation with Perry Parendo, a seasoned expert in product development and project management within the MedTech sector. Host Etienne Nichols and Perry delve into the challenges and opportunities facing medical device development, emphasizing the critical role of agile pract…

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Medical Device News April 2024 Regulatory Update

2M ago

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Sponsor: Medboard: https://www.medboard.com/ EU MDR and IVDR national languages update – France accepts English MDR: https://health.ec.europa.eu/document/download/aa9760e3-c864-4173-8b16-d790dac66d74_en?filename=md_sector_lang-req-table-mdr.pdf IVDR: https://health.ec.europa.eu/document/download/1e312d8f-8b34-45da-a5fa-1918ba618aca_en?filename=md_s…

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Software Sales VS Medical Device Sales with Will Padilla 50:30

2M ago50:30

50:30

Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medical-device-sales First Year in Ebook: https://www.newtomedicaldevicesales.com/prod…

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How to benefit from Surveys to build Clinical Evidence?

2M ago

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Since EU MDR and IVDR launched, there is a phenomenon that raised which is the use of surveys to gather clinical data. So we wanted to share with you how to do this right and what you should be careful on. So listen to Cesare Magri from 4BetterDevices who will tell us more about surveys in the Medical Device field. Who is Cesare Magri? Cesare has a…

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2024-05: Was der EU AI Act für Medizinproduktehersteller bedeutet 24:45

2M ago24:45

24:45

Eine erste Einordnung der neuen EU-Verordnung mit Dr. Till Klein Anfang März 2024 hat die EU den AI Act, die Verordnung zu Produkten mit künstlicher Intelligenz, veröffentlicht. In dieser Podcast-Episode geht der AI-Act-Experte Dr. Till Klein im Gespräch mit Prof. Johner Fragen nach wie: Was ist das Ziel des AI Acts? Welche konkreten Anforderungen …

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Being a Woman in Medical Device Sales with Roxy Tirado 49:04

2M ago49:04

49:04

Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medical-device-sales First Year in Ebook: https://www.newtomedicaldevicesales.com/prod…

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#358: FDAs Voluntary Improvement Program 28:55

2M ago28:55

28:55

In this episode of the Global Medical Device Podcast, host Etienne Nichols sits down with Kim Kaplan from ISACA at the MD&M West trade show in Anaheim, California, to discuss the pivotal Voluntary Improvement Program (VIP). This conversation sheds light on how the program, stemming from FDA’s Case for Quality initiative, utilizes the Capability Mat…

1
How to do Postmarketing Surveillance the right way?

2M ago

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The EU MDR and IVDR is a bit more demanding on Postmarketing Surveillance. In this episode we will explain to you from the eye of an auditor what they want to see and how you can avoid some mistakes that are always identified. Who is Steve Curran? Dr Steve Curran has over 20 years experience in the medical device industry both as an engineer and le…

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2024-04: Mit Medizinprodukten schnell im großen US-Markt Umsätze erzielen 16:28

2M ago16:28

16:28

Hilfestellung für die FDA-Zulassung von Medizinprodukten Der US-Markt wird für europäische Hersteller immer attraktiver. Denn zum einen gelingt es den Herstellern, schneller und einfacher die regulatorischen Anforderungen zu erfüllen und ihre Produkte in den Markt zu bringen. Zum anderen ist der US-Markt sehr groß und teilweise homogener als der eu…

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Medical Device Sales Rep At 22 Years Old with Garrett Wilson 35:07

2M ago35:07

35:07

Website: https://www.newtomedicaldevicesales.com Break into Medical Device Sales Online Course: https://courses.newtomedicaldevicesales.com Guide for Breaking into Medical Device Sales Ebook: https://www.newtomedicaldevicesales.com/product/guide-for-breaking-into-medical-device-sales First Year in Ebook: https://www.newtomedicaldevicesales.com/prod…

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Learn more about FDA QMSR alignment with ISO 13485

2M ago

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The FDA announced the alignment of QMSR to the ISO 13485 standard. So now the question is: What does it change for me? Do you need to update your full QMS? Will you need to go through another audit or inspection? Is this really a revolution? Naveen Agarwal from Exceed will answer this question. So don’t miss this episode to know more about QMSR. Wh…

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Medical Device Podcastok

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