Podcasts Business Medical Device made Easy Podcast
Medical Device made Easy Podcast

Medical Device made Easy Podcast

131 episodes

On the Medical Device made Easy Podcast you'll learn how to place a compliant medical device on the market. I will share with you my experience and one of my guests. I am Monir El Azzouzi a Medical Device Expert specialized in Quality and Regulatory Affairs. I am also the founder of the Medical Device blog called Easy Medical Device where I try to teach to people the basics of Medical Devices. One of my Motto is "Would I give this product to a Member of my family" and I try to share this philosophy with all my community. If you are trying to learn more or to change your career to enter the medical device world, you should be part of my community. I will be your guide and will help you reach your objectives. Regulation is changing all over the world and this is hitting all medical device manufacturers. They need your help so learn and apply.

Podcasts

Medical Device News january 2024 Regulatory Update

Published: Jan. 10, 2024, midnight
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Regulatory Maturity Model Heatmap (MEDICA 2023)

Published: Jan. 2, 2024, midnight
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Life of QA RA Podcasters?

Published: Dec. 26, 2023, midnight
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Why should you invest in your Regulatory Team?

Published: Dec. 18, 2023, 11:35 p.m.
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What is Usability for Medical Devices?

Published: Dec. 12, 2023, midnight
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Medical Device News: December 2023 Regulatory Update

Published: Dec. 5, 2023, midnight
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What is the situation regarding digitalization in Medtech?

Published: Nov. 28, 2023, 8:10 a.m.
Duration: N/A

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How to find your Predicate Device for your 510K Submission?

Published: Nov. 21, 2023, midnight
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How to CE certify a Calculator, Risk Score...?

Published: Nov. 14, 2023, midnight
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Medical Device News November 2023 Regulatory Update

Published: Nov. 9, 2023, midnight
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Validate your Iphone, Samsung Galaxy, Huawei... for your Software

Published: Oct. 31, 2023, midnight
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Afrisummit 2023 Interviews Part 2 Egypt Situation

Published: Oct. 24, 2023, midnight
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Afrisummit 2023 Interviews Part 1

Published: Oct. 17, 2023, midnight
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What are some pitfalls to avoid during Software Design?

Published: Oct. 10, 2023, midnight
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October 2023 Regulatory Update

Published: Oct. 4, 2023, midnight
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What is the EUDAMED Updates?

Published: Sept. 26, 2023, midnight
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Interviews on Being The PRRC (Part 2)

Published: Sept. 19, 2023, midnight
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MEDICAL DEVICE NEWS SEPTEMBER 2023 Regulatory Update

Published: Sept. 6, 2023, 7:51 a.m.
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How to perform your Cleaning Validation in practice?

Published: Aug. 29, 2023, midnight
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What are the Acceptance Criteria for your Clinical Evaluation?

Published: Aug. 22, 2023, 1:07 a.m.
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Why you should automate your Software validation?

Published: Aug. 15, 2023, midnight
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Hire your QA RA person with no Budget

Published: Aug. 8, 2023, 8:02 a.m.
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Who should be on your Risk Management Dream Team?

Published: Aug. 1, 2023, midnight
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Artificial Intelligence in the Medical Device Industry

Published: July 25, 2023, midnight
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Validation of Quality Software in Medical Devices

Published: July 18, 2023, midnight
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How to register Medical Devices in Saudi Arabia?

Published: July 11, 2023, 1 a.m.
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Medical Device News July 2023 Regulatory Update

Published: July 4, 2023, 8:15 a.m.
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What should you know on UKCA extension

Published: June 27, 2023, 12:01 a.m.
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How to connect Software dev and QA RA Team

Published: June 20, 2023, midnight
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The great misunderstanding of EU MDR amendments

Published: June 13, 2023, midnight
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Medical Device News -June 2023 regulatory update

Published: June 8, 2023, midnight
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How to master Regulatory Intelligence?

Published: May 30, 2023, midnight
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What if your Medical Device Company goes Bankrupt?

Published: May 23, 2023, midnight
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Technical Files Inconsistencies Identified by Notified Bodies

Published: May 16, 2023, midnight
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The truth about the UK vs EU situation

Published: May 9, 2023, 12:23 a.m.
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Medical Device news May 2023 Regulatory Update

Published: May 5, 2023, 1 a.m.
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Transition to Agile for Software as Medical Device

Published: April 25, 2023, 1 a.m.
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Prepare your audit like a PRO

Published: April 18, 2023, midnight
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What is a SOUP for your Software Development?

Published: April 11, 2023, 1 a.m.
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How to perform Risk Management for a Software ?

Published: March 28, 2023, midnight
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How to create a Proactive Postmarketing Surveillance? [EU MDR]

Published: March 21, 2023, midnight
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What you should know about Vigilance Reporting for Medical Devices?

Published: March 14, 2023, midnight
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Medical Device News: March 2023 Regulatory Update

Published: March 8, 2023, midnight
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Prepare your transition from Class I to Class Ir

Published: Feb. 28, 2023, midnight
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SaMD international reach What to consider?

Published: Feb. 21, 2023, midnight
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Biological Evaluation: Top Big mistakes

Published: Feb. 14, 2023, midnight
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Medical Device News: February 2023 Regulatory Update

Published: Feb. 6, 2023, 11:46 p.m.
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How to do Post-Marketing Surveillance in the US (vs EU)?

Published: Jan. 31, 2023, 12:31 a.m.
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How to evaluate Benefit-Risk Ratio for Medical Devices?

Published: Jan. 24, 2023, 1 a.m.
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Breaking News: EU MDR Extension Proposal is out for consultation

Published: Jan. 17, 2023, 1 a.m.
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How to improve the relationship between QA RA and Marketing?

Published: Jan. 10, 2023, midnight
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Medical Device News: January 2023 Regulatory Update

Published: Jan. 3, 2023, 7:46 a.m.
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Grow your LinkedIn Profile with Karandeep Badwal

Published: Dec. 27, 2022, 2:30 a.m.
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Is EU MDR extended? with Erik Vollebregt

Published: Dec. 20, 2022, 12:50 a.m.
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MDCG, Team-NB, BVMed & Team-PRRC tell you all about PRRC

Published: Dec. 13, 2022, 1 a.m.
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Medical Device News December 2022 Regulatory Update

Published: Dec. 6, 2022, 7:29 a.m.
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How to choose the best Sterilization Method for Medical Devices?

Published: Nov. 29, 2022, midnight
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Why Risk Management is important to Medical Device development?

Published: Nov. 22, 2022, midnight
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Regulatory Pathway: How to reach the US market? [510k exempt]

Published: Nov. 15, 2022, midnight
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Your Software/IVD clinical report is completely WRONG!

Published: Nov. 8, 2022, midnight
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Medical Device News November 2022 Regulatory Update

Published: Nov. 1, 2022, 1 a.m.
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Can you go to Jail as a PRRC? [Elem Ayne]

Published: Oct. 25, 2022, 1 a.m.
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How to be MDSAP certified for your Medical Devices?

Published: Oct. 18, 2022, 1 a.m.
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Medical Device News October 2022 Regulatory Update

Published: Oct. 11, 2022, 12:30 a.m.
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What do Clients, Followers, Team, ... think of Easy Medical Device?

Published: Oct. 4, 2022, midnight
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How to select your Notified Body and understand the full process?

Published: Sept. 27, 2022, midnight
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How to become the best PRRC ever? [Ronald Boumans]

Published: Sept. 20, 2022, midnight
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Why do you need an Initial Importer for the US Market?

Published: Sept. 13, 2022, 12:20 a.m.
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Medical Device News: September 2022 Regulatory Update

Published: Sept. 6, 2022, 2:50 a.m.
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SaMD or SiMD How to create your Design Dossier?

Published: Aug. 30, 2022, midnight
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New Blue Guide What is the impact on Medical Devices?

Published: Aug. 23, 2022, 1 a.m.
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Why are we not Discontinuing your Products?

Published: Aug. 16, 2022, 1 a.m.
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When you think 510k but FDA says DeNovo with Spencer Jones

Published: Aug. 9, 2022, midnight
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How to create your Technical Documentation? [EU MDR and IVDR]

Published: Aug. 2, 2022, midnight
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Maybe you need a Cleanroom? Lets check with Philippe Bourbon

Published: July 26, 2022, midnight
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AI Act vs EU MDR 2017/745 are they compatible? [Erik Vollebregt]

Published: July 19, 2022, midnight
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Medtech Europe Forum interviews (MDR, EUDAMED, CER & MECOMED)

Published: July 12, 2022, 2:50 a.m.
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Medical Device News July 2022 Regulatory Update

Published: July 5, 2022, 2 a.m.
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Attention! 1 year before UKCA is the law for Medical Devices in the UK

Published: June 28, 2022, midnight
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Why is it great for Importers to be ISO 13485 certified? [Cristina Miroescu]

Published: June 21, 2022, midnight
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What are some Quality Common Mistakes? [Karandeep Badwal]

Published: June 14, 2022, 2 a.m.
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Medical Device News: June 2022 Regulatory Update

Published: June 7, 2022, 2:30 a.m.
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Lets introduce you to our eQMS SmartEye with Anindya Mookerjea

Published: May 31, 2022, 12:43 a.m.
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What to learn about the EU Medical Device situation? [Erik Vollebregt]

Published: May 24, 2022, 12:45 a.m.
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What happens after the IVDR Date of Application with Colm ORourke

Published: May 17, 2022, midnight
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How to certify your Software as a Medical Device? (SaMD)

Published: May 10, 2022, midnight
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Medical Device News: May 2022 Regulatory Update

Published: May 3, 2022, 12:50 a.m.
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Training Process What are the mistakes to avoid? [ISO 13485]

Published: April 26, 2022, 12:30 a.m.
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How your PMCF is evaluated by your Notified Body? [Matthias Fink]

Published: April 19, 2022, 2 a.m.
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How to prepare an Audit with a Front Room & a Back Room?

Published: April 12, 2022, 1 a.m.
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Medical Device News: April 2022 Update

Published: April 5, 2022, 2 a.m.
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What are the surprises during MDR & IVDR transition? [Erik Vollebregt]

Published: March 29, 2022, midnight
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How to sell Medical Devices online in the EU and US?

Published: March 22, 2022, midnight
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What lesson did we learn doing Clinical Evaluations? [Cesare Magri]

Published: March 15, 2022, 12:43 a.m.
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Why do we need the Common Specification for Class D IVDR?

Published: March 8, 2022, midnight
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Medical Device News March 2022 Regulatory Update

Published: March 1, 2022, 1 a.m.
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Why would you need a Swiss Authorised Representative and Importer?

Published: Feb. 22, 2022, 1 a.m.
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How to be great at Management Reviews? [ISO 13485]

Published: Feb. 15, 2022, 12:30 a.m.
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Why Design History File (DHF) is so important? [Alexandros Savvidis]

Published: Feb. 8, 2022, midnight
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Medical Device News: February 2022 Regulatory Update

Published: Feb. 1, 2022, midnight
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MDCG 2021-27 Placing on the market & Re-labelling with Erik Vollebregt

Published: Jan. 25, 2022, midnight
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How to interview your QA RA Candidates? [Mitch Robbins]

Published: Jan. 18, 2022, midnight
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How to accelerate your Laboratory Test Results? [Christoph Lindner]

Published: Jan. 11, 2022, 2 a.m.
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Medical Device News January 2022 [Happy New Year]

Published: Jan. 4, 2022, 3 a.m.
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What happened in 2021? Summary for the Medical Device Industry

Published: Dec. 28, 2021, 2 a.m.
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The Step-by-Step recipe to get MDR & IVDR Certified

Published: Dec. 21, 2021, 2 a.m.
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Which devices cannot be Custom-made? [Erik Vollebregt]

Published: Dec. 14, 2021, midnight
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Medical Device News: December 2021 Regulatory Update

Published: Dec. 7, 2021, 2 a.m.
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Lets unleash MDR Classification surprises [MDR 2017/745]

Published: Nov. 30, 2021, 2 a.m.
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How to approach your Notified Bodies? [Dr. Royth von Hahn TUV SUD]

Published: Nov. 23, 2021, 2 a.m.
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Is it possible to Private Label a Medical Device under MDR & IVDR?

Published: Nov. 16, 2021, 2:18 a.m.
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How to improve your QA RA Communication with Lesley Worthington?

Published: Nov. 9, 2021, 2 a.m.
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Medical Device News November 2021 latest update

Published: Nov. 2, 2021, 3 a.m.
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How does the EU Commission plan to save IVDR 2017/746?

Published: Oct. 26, 2021, 1:20 a.m.
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How to comply with MDR when products contain CMR Substances?

Published: Oct. 19, 2021, 2 a.m.
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EUDAMED Update: Should you register your medical devices now?

Published: Oct. 12, 2021, 2 a.m.
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Medical Device News October 2021 Regulatory Update

Published: Oct. 5, 2021, 2:30 a.m.
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Why does an Importer/Distributor need to appoint a Notified Body?

Published: Sept. 28, 2021, midnight
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How to collect Clinical Data within the 21st Century [Jon Bergsteinsson]

Published: Sept. 21, 2021, 1 a.m.
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How to manage the IVDR transition period? [IVDR 2017/745]

Published: Sept. 14, 2021, midnight
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Is it a good idea to sue my Notified Body? [Erik Vollebregt]

Published: Sept. 7, 2021, midnight
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Medical Device News September 2021 Latest Updates

Published: Aug. 31, 2021, midnight
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How to Certify a Software as Medical Device? (Dr. Abtin Rad TUV SUD)

Published: Aug. 24, 2021, midnight
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Better to be a Consultant or a Full-time employee? [Lifescience industry]

Published: Aug. 17, 2021, midnight
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What can we learn from the first MDR audits? [Martin Witte -TUV SUD]

Published: Aug. 10, 2021, midnight
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Medical Device News August 2021 Regulatory Update [MDR & IVDR]

Published: Aug. 3, 2021, midnight
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How to implement Vigilance Reporting for MDR and IVDR?

Published: July 27, 2021, midnight
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System and Procedure Pack the RETURN with Erik Vollebregt

Published: July 20, 2021, midnight
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How to interpret the first Expert Panel Opinion? [Bassil Akra]

Published: July 13, 2021, midnight
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Medical Device News: The July 2021 Update [MDR IVDR FDA SFDA]

Published: July 6, 2021, midnight
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How to build your State-of-the-art for your Medical Devices?

Published: June 29, 2021, midnight
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How Intellectual Property is linked to the Medical Device Regulation?

Published: June 22, 2021, midnight
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How to perform a good Clinical Investigation with Helene Quie

Published: June 15, 2021, midnight
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How to perform a Biological Evaluation for your Medical Device?

Published: June 8, 2021, midnight
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Medical Device News June 2021 Update [EU MDR Date of Application]

Published: June 1, 2021, midnight
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EU MDR Survey: What is the Industrys opinion? [Catherine Higginson]

Published: May 25, 2021, midnight
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MDR is coming so brace yourself with Erik Vollebregt

Published: May 18, 2021, midnight
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FDA: Is the Emergency Use Authorization worth it? (EUA)

Published: May 11, 2021, 1 a.m.
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Medical Device News May 2021 Update [EU MDR 2017/745]

Published: May 4, 2021, midnight
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Checklist What is important before the EU MDR Date of Application?

Published: April 27, 2021, midnight
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How to perform correctly a Merger & Acquisition during the MDR transition?

Published: April 20, 2021, midnight
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Will it be really difficult for IVD manufacturers? [IVDR 2017/746]

Published: March 30, 2021, midnight
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How to create a Label under MDR? (Questions & Answers)

Published: March 23, 2021, midnight
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How System and Procedure Pack are regulated under EU MDR?

Published: March 16, 2021, midnight
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How to import your Medical Devices with an Independent Importer?

Published: March 9, 2021, midnight
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What is the Medical Device News? [March 2021 update]

Published: March 2, 2021, midnight
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The best design methods for successful development? [Jon Speer]

Published: Feb. 23, 2021, midnight
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How to find a QA RA job for Medical Devices? [Karandeep Badwal]

Published: Feb. 16, 2021, midnight
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What is the QA RA Mindset with Michelle Lott

Published: Feb. 9, 2021, midnight
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February 2021 Update Medical Devices Remote Audit by the EU

Published: Feb. 2, 2021, midnight
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How to perform your PMS more easily with Ivan Perez Chamorro?

Published: Jan. 26, 2021, midnight
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How to get the MDR certification for Artificial Intelligence Softwares?

Published: Jan. 19, 2021, midnight
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How to register a Medical Device in Israel? (Liat Nadel)

Published: Jan. 12, 2021, midnight
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Medical Device News January 2021 Update (Monir El Azzouzi)

Published: Jan. 5, 2021, 9 a.m.
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How Easy Medical Device can help you? (Monir El Azzouzi)

Published: Dec. 28, 2020, midnight
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How to deal with Significant Changes within MDR & IVDR with Martin Witte

Published: Dec. 21, 2020, midnight
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How to register a Medical Device in Mexico? [Josue Garza]

Published: Dec. 14, 2020, midnight
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Medical Device News: What happened in November 2020?

Published: Dec. 7, 2020, midnight
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Is it Easy for a Notified Body to get EU MDR accredited?

Published: Nov. 30, 2020, midnight
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How a Quality & Regulatory training can help you? [Sofmedica]

Published: Nov. 23, 2020, midnight
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Do you need an Expert Panel for your Medical Devices? [Bassil Akra]

Published: Nov. 16, 2020, midnight
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What are Common Specifications under EU MDR & IVDR?

Published: Nov. 9, 2020, midnight
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Weve reached episode 100 What happened for the last 2 years?

Published: Nov. 2, 2020, midnight
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How to certify a self-testing device under IVDR? [Erik Vollebregt]

Published: Oct. 26, 2020, midnight
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What is the cost of EU MDR 2017/745? [Catherine Higginson]

Published: Oct. 19, 2020, midnight
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How to register your Medical Device in the ASEAN region?

Published: Oct. 12, 2020, midnight
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The latest news on Brexit, Swixit and EU MDR [Medical Device News]

Published: Oct. 5, 2020, midnight
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How to register ATMP-Device combination products?

Published: Sept. 28, 2020, midnight
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How to get some help from Medical Device Regulators with Cliff Bleustein

Published: Sept. 21, 2020, midnight
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How can GDPR impact Medical Devices with Erik Vollebregt

Published: Sept. 14, 2020, midnight
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Be successful at your MDR and IVDR audit with Martin Witte

Published: Sept. 7, 2020, midnight
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Medical Device News August 2020 Review (Monir El Azzouzi)

Published: Aug. 31, 2020, midnight
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How to switch quickly to a Virtual Conference with TOPRA

Published: Aug. 24, 2020, midnight
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Best practice for Device Testing with Michael Wetherington

Published: Aug. 17, 2020, midnight
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Best overview of IEC 60601 for Medical Device electrical equipment

Published: Aug. 10, 2020, midnight
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Medical Device News July 2020 Update on Quality and Regulatory for Medical Devices

Published: Aug. 3, 2020, midnight
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Learn UDI code for Medical Devices with Sylvia Reingardt

Published: July 27, 2020, midnight
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Understand IEC 62304 for Medical Device Software with Adnan Ashfaq

Published: July 20, 2020, midnight
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How to become a PRRC with TEAM-PRRC (EU MDR & IVDR)

Published: July 13, 2020, midnight
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Medical Device News June 2020 Update

Published: July 6, 2020, midnight
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The secrets to being EU MDR certified with Shokoufeh Khodabandeh

Published: June 29, 2020, midnight
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How to perform your Process Validation with Adnan Ashfaq (IQ OQ PQ)

Published: June 22, 2020, midnight
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How to execute your Internal Audits? (Medical Device companies)

Published: June 15, 2020, midnight
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Medical Device News May 2020 Review with Monir El Azzouzi

Published: June 8, 2020, midnight
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What means Sufficient Clinical Data with Bassil Akra (EU MDR)

Published: June 1, 2020, midnight
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What is the Notified Body situation? (Bassil Akra from TUV SUD)

Published: May 25, 2020, midnight
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How to get ISO 13485 certified? (Quality Management System)

Published: May 18, 2020, midnight
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How to get your Digital Health Application reimbursed in Germany? (DIGA)

Published: May 11, 2020, midnight
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Medical Device News April 2020 Regulatory Update

Published: May 4, 2020, midnight
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How to calculate your sample size with Jon Bergsteinsson

Published: April 27, 2020, midnight
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The 1-year delay for the EU MDR 2017/745 with Erik Vollebregt

Published: April 20, 2020, midnight
Duration: N/A

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Medical Device School Why are Staff hiding problems to QA & RA?

Published: April 15, 2020, midnight
Duration: N/A

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MDR & Drug-Device Combination Products with Theresa Jeary

Published: April 13, 2020, midnight
Duration: N/A

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Medical Device News March 2020 Review (EU MDR)

Published: April 6, 2020, midnight
Duration: N/A

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What is a Significant Change for your Medical Device? with Erik Vollebregt

Published: March 30, 2020, midnight
Duration: N/A

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All about Class Is, Im and Ir with Elem Ayne (EU MDR 2017/745)

Published: March 23, 2020, midnight
Duration: N/A

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Cybersecurity for your Medical Devices with Erik Vollebregt

Published: March 16, 2020, midnight
Duration: N/A

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Medical Device Regulatory Update February 2020

Published: March 9, 2020, midnight
Duration: N/A

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Do your Economic Operators need a Quality Management System?

Published: March 4, 2020, midnight
Duration: N/A

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Create your intended purpose with Cesare Magri (Medical Device)

Published: March 2, 2020, midnight
Duration: N/A

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Medical Device School: What should verify your Economic Operators?

Published: Feb. 26, 2020, midnight
Duration: N/A

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Clinical Data for Low Risk Medical Devices with Robert van Boxtel

Published: Feb. 24, 2020, midnight
Duration: N/A

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Medical Device School Who controls your Economic Operators?

Published: Feb. 19, 2020, midnight
Duration: N/A

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Are Brexit, Swixit, and Turkxit a reality? with Erik Vollebregt

Published: Feb. 17, 2020, midnight
Duration: N/A

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Medical Device School Who are your Economic Operators?

Published: Feb. 12, 2020, midnight
Duration: N/A

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Swixit or not Swixit? this is the question with Ronald Boumans

Published: Feb. 10, 2020, midnight
Duration: N/A

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Medical Device School Process Validation or Verification?

Published: Feb. 5, 2020, midnight
Duration: N/A

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Episode 61 Medical Device Regulatory Update: January 2020

Published: Feb. 3, 2020, midnight
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How to register your Device in Brazil with Tania Aprigliano? (ANVISA)

Published: Jan. 27, 2020, midnight
Duration: N/A

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Why is it Awesome to work in a Quality or Regulatory affairs job?

Published: Jan. 22, 2020, midnight
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How to create a QMS compliant to MDR with Stefan Bolleininger

Published: Jan. 20, 2020, midnight
Duration: N/A

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How to register your Medical Device through 510k with Michelle Lott

Published: Jan. 13, 2020, midnight
Duration: N/A

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Medical Device School: How to audit your Suppliers?

Published: Jan. 8, 2020, midnight
Duration: N/A

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Post-Marketing Clinical Follow-up with Helene Quie (PMCF)

Published: Jan. 6, 2020, midnight
Duration: N/A

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I wish you a Happy New Year 2020 with Monir El Azzouzi

Published: Dec. 30, 2019, midnight
Duration: N/A

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6 ways to collect Clinical Data with David Rutledge

Published: Dec. 23, 2019, midnight
Duration: N/A

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Class I Medical Devices under MDR with Erik Vollebregt (PART 2)

Published: Dec. 16, 2019, midnight
Duration: N/A

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Corrigendum 2 Changes for Class I Devices with Erik Vollebregt (Part 1)

Published: Dec. 9, 2019, midnight
Duration: N/A

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How to evaluate your Medical Devices in 3 Steps with Heikki Pitkanen?

Published: Dec. 2, 2019, midnight
Duration: N/A

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Responsibility of a Distributor in MDR & IVDR with Nicolaj Nitzsch

Published: Nov. 25, 2019, midnight
Duration: N/A

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Medical Device School: Product Development or Documentation creation?

Published: Nov. 21, 2019, midnight
Duration: N/A

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EUDAMED is delayed, so What? with Richard Houlihan

Published: Nov. 18, 2019, midnight
Duration: N/A

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Literature Search for your CER with Ed Drower

Published: Nov. 11, 2019, 1 a.m.
Duration: N/A

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Medical Device School: How to build a Gap Assessment Tool?

Published: Nov. 7, 2019, midnight
Duration: N/A

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How to validate an eQMS with Jacob Sjorslev

Published: Nov. 4, 2019, midnight
Duration: N/A

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How to implement an eQMS with Jacob Sjorslev

Published: Oct. 28, 2019, midnight
Duration: N/A

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Medical Device School Most important issues on your CAPA (ISO 13485)

Published: Oct. 24, 2019, midnight
Duration: N/A

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Medical Device Disruptions at Hospitals with Stefan Krojer

Published: Oct. 20, 2019, 11:01 a.m.
Duration: N/A

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5 FDA Myths for Start-Ups with Justin Bushko

Published: Oct. 14, 2019, midnight
Duration: N/A

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GDPR & MDR for Medical Applications with Jovan Stevovic

Published: Oct. 6, 2019, 10:38 p.m.
Duration: N/A

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Register your Medical Device in the US with Michelle Lott (FDA)

Published: Sept. 29, 2019, 10:59 p.m.
Duration: N/A

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New rules for the In-Vitro Diagnostic Industry with Maurizio Suppo

Published: Sept. 21, 2019, 11:01 p.m.
Duration: N/A

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Learn Post Market Surveillance with Natasha Bankowski

Published: Sept. 15, 2019, 11:02 p.m.
Duration: N/A

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Product Equivalence for Clinical Evaluation Report (CER) with Helene Quie

Published: Sept. 7, 2019, 11:10 p.m.
Duration: N/A

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Episode 39 Networking at Medical Device events with Lynda Wight

Published: Sept. 1, 2019, 10:30 p.m.
Duration: N/A

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Episode 38 Be the Best Candidate Ever with Mitch Robbins

Published: Aug. 26, 2019, midnight
Duration: N/A

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Episode 37 Usability & Human Factor with Sharon Ayd

Published: Aug. 19, 2019, midnight
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Episode 36 How to choose your PRRC with Erik Vollebregt

Published: Aug. 12, 2019, midnight
Duration: N/A

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Episode 35 Digitalization of QA RA with Michael Kania

Published: Aug. 5, 2019, midnight
Duration: N/A

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Episode 34 Real-World Data for Medical Devices with Alethea Wieland

Published: July 29, 2019, midnight
Duration: N/A

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Episode 33 Notified Bodies Lay Down Service with Erik Vollebregt

Published: July 22, 2019, midnight
Duration: N/A

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Episode 32 Pakistan Registration Process with Muhammad Sohail

Published: July 14, 2019, 10:59 p.m.
Duration: N/A

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Episode 31 First Regulatory Affairs Job with Karandeep Badwal

Published: July 6, 2019, 11:05 p.m.
Duration: N/A

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Episode 30 Promotional Compliance with Darshan Kulkarni

Published: June 30, 2019, 10:59 p.m.
Duration: N/A

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Episode 29 5 Steps to create a QMS with Jason Lim

Published: June 23, 2019, 10:59 p.m.
Duration: N/A

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Episode 28 OBL & OEM with Stefan Bolleininger Part 2

Published: June 16, 2019, 11:01 p.m.
Duration: N/A

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Episode 27 OEM & OBL Model with Stefan Bolleininger [Part 1]

Published: June 10, 2019, 1:30 a.m.
Duration: N/A

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Episode 26 IVDR preparation with Andreas Stange

Published: June 3, 2019, 3:30 a.m.
Duration: N/A

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Episode 25 EUDAMED secrets with Richard Houlihan

Published: May 27, 2019, 3 a.m.
Duration: N/A

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Episode 24 Myths about consultants with Thomas McMann

Published: May 20, 2019, 4 a.m.
Duration: N/A

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Episode 23- TOP 10 criteria to select a CRO with Alethea Wieland

Published: May 13, 2019, 5 a.m.
Duration: N/A

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Episode 22 Clinical Trial with Alethea Wieland

Published: May 6, 2019, 5 a.m.
Duration: N/A

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Episode 21 How to master Regulatory Affairs with Samantha Alsbury

Published: April 29, 2019, 5 a.m.
Duration: N/A

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Episode 20 What is a Blockchain with Khuram Malik

Published: April 22, 2019, 5:30 a.m.
Duration: N/A

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Episode 19 Rule 11 for Software Devices with Cyrille Michaud

Published: April 15, 2019, 3:30 a.m.
Duration: N/A

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Episode 18 QA RA Recruitment situation with Petra Ognjenovic

Published: April 8, 2019, 2 a.m.
Duration: N/A

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Episode 17 Unannounced audit stories with Florent Guyon

Published: April 1, 2019, 4 a.m.
Duration: N/A

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Episode 16 From Disease to a Medical Device with Sean Hamilton

Published: March 25, 2019, 2 a.m.
Duration: N/A

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Episode 15 MDR & IVDR discussion with Erik Vollebregt Part 2

Published: March 18, 2019, 3 a.m.
Duration: N/A

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Episode 14 MDR & IVDR stories with Erik Vollebregt (Part 1)

Published: March 11, 2019, 2 a.m.
Duration: N/A

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Episode 13 Brexit Talk with Richard Young

Published: March 4, 2019, 5 a.m.
Duration: N/A

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Episode 12 How to create an ISO Standard with Marcelo Antunes

Published: Feb. 25, 2019, 5 a.m.
Duration: N/A

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Episode 11 Medical Device Software Validation

Published: Feb. 17, 2019, 9:40 a.m.
Duration: N/A

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Episode 10 Understand MDSAP with Angelina Hakim

Published: Feb. 11, 2019, 6 a.m.
Duration: N/A

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Episode 9 Entrepreneurial journey with Ivan Perez Chamorro

Published: Feb. 3, 2019, 10 a.m.
Duration: N/A

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Episode 8 From Correction to Prevention with ODIAC

Published: Jan. 27, 2019, 11:03 a.m.
Duration: N/A

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Episode 7 Make your KPIs Green again

Published: Jan. 20, 2019, 11:55 a.m.
Duration: N/A

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Episode 6 What are the 6 types of Medical Device Audits

Published: Jan. 12, 2019, 3:02 p.m.
Duration: N/A

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Episode 5 Medtech Prediction 2019

Published: Jan. 6, 2019, 11:42 a.m.
Duration: N/A

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Episode 4 UDI for Unique Device Identification

Published: Dec. 29, 2018, 9:21 p.m.
Duration: N/A

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Episode 3 Is my Product a Medical Device in Europe?

Published: Dec. 20, 2018, 2:04 p.m.
Duration: N/A

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Episode 2 New EU Medical Device Regulation MDR 2017/745

Published: Dec. 16, 2018, 5:43 p.m.
Duration: N/A

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Episode 1 Introduction to the Medical Device made Easy Podcast

Published: Dec. 14, 2018, 11:04 p.m.
Duration: N/A

Listed in: Business