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Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

Why and how to build a Quality Culture?

0 secs; April 22, 2024

What is the impact of AI Act on Medical Devices?

0 secs; April 15, 2024

Radiation Sterilisation Master File (ISO 11137 & 11607)

0 secs; April 08, 2024

Medical Device News April 2024 Regulatory Update

0 secs; April 03, 2024

How to benefit from Surveys to build Clinical Evidence?

0 secs; March 25, 2024

How to do Postmarketing Surveillance the right way?

0 secs; March 18, 2024

Learn more about FDA QMSR alignment with ISO 13485

0 secs; March 11, 2024

Medical Device News March 2024 Regulatory Update

0 secs; March 05, 2024

New EU Proposal – EUDAMED, IVDR & Shortage

0 secs; February 26, 2024

Will EtO gaz become a Medical Device?

0 secs; February 19, 2024

How to get your interview prepared?

0 secs; February 12, 2024

Medical Device News february 2024 Regulatory Update

0 secs; February 07, 2024

Why you should use Pre-Submission or Q-Sub with FDA?

0 secs; January 29, 2024

You are not the Physical Manufacturer, can you be MDR certified?

0 secs; January 22, 2024

MEDICA 2023 – InterviewS with Startups, Service Providers, Notified Bodies…

0 secs; January 18, 2024

WARNING! APPLY TO YOUR NOTIFIED BODY NOW!

0 secs; January 15, 2024

Medical Device News – january 2024 Regulatory Update

0 secs; January 09, 2024

Regulatory Maturity Model – Heatmap (MEDICA 2023)

0 secs; January 01, 2024

Life of QA RA Podcasters?

0 secs; December 25, 2023

Why should you invest in your Regulatory Team?

0 secs; December 18, 2023

What is Usability for Medical Devices?

0 secs; December 11, 2023

Medical Device News: December 2023 Regulatory Update

0 secs; December 04, 2023

What is the situation regarding digitalization in Medtech?

0 secs; November 28, 2023

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

0 secs; November 20, 2023

How to CE certify a Calculator, Risk Score…?

0 secs; November 13, 2023

Medical Device News – November 2023 Regulatory Update

0 secs; November 08, 2023

Validate your Iphone, Samsung Galaxy, Huawei… for your Software

0 secs; October 30, 2023

Afrisummit 2023 Interviews Part 2 – Egypt Situation

0 secs; October 23, 2023

Afrisummit 2023 Interviews Part 1

0 secs; October 16, 2023

What are some pitfalls to avoid during Software Design?

0 secs; October 09, 2023

October 2023 Regulatory Update

0 secs; October 03, 2023

What is the EUDAMED Updates?

0 secs; September 25, 2023

Interviews on Being The PRRC (Part 2)

0 secs; September 18, 2023

MEDICAL DEVICE NEWS – SEPTEMBER 2023 Regulatory Update

0 secs; September 06, 2023

How to perform your Cleaning Validation in practice?

0 secs; August 28, 2023

What are the Acceptance Criteria for your Clinical Evaluation?

0 secs; August 21, 2023

Why you should automate your Software validation?

0 secs; August 14, 2023

Hire your QA RA person with no Budget

0 secs; August 08, 2023

Who should be on your Risk Management Dream Team?

0 secs; July 31, 2023

Artificial Intelligence in the Medical Device Industry

0 secs; July 24, 2023

Validation of Quality Software in Medical Devices

0 secs; July 17, 2023

How to register Medical Devices in Saudi Arabia?

0 secs; July 10, 2023

Medical Device News – July 2023 Regulatory Update

0 secs; July 04, 2023

What should you know on UKCA extension

0 secs; June 26, 2023

How to connect Software dev and QA RA Team

0 secs; June 19, 2023

The great misunderstanding of EU MDR amendments

0 secs; June 12, 2023

Medical Device News -June 2023 regulatory update

0 secs; June 07, 2023

How to master Regulatory Intelligence?

0 secs; May 29, 2023

What if your Medical Device Company goes Bankrupt?

0 secs; May 22, 2023

Technical Files Inconsistencies Identified by Notified Bodies

0 secs; May 15, 2023

The truth about the UK vs EU situation

0 secs; May 08, 2023

Medical Device news – May 2023 Regulatory Update

0 secs; May 04, 2023

Transition to Agile for Software as Medical Device

0 secs; April 24, 2023

Prepare your audit like a PRO

0 secs; April 17, 2023

What is a SOUP for your Software Development?

0 secs; April 10, 2023

Medical Device News – March 2023 Regulatory Update

0 secs; April 03, 2023

How to perform Risk Management for a Software ?

0 secs; March 27, 2023

How to create a Proactive Postmarketing Surveillance? [EU MDR]

0 secs; March 20, 2023

What you should know about Vigilance Reporting for Medical Devices?

0 secs; March 13, 2023

Medical Device News: March 2023 Regulatory Update

0 secs; March 07, 2023

Prepare your transition from Class I to Class Ir

0 secs; February 27, 2023

SaMD international reach – What to consider?

0 secs; February 20, 2023

Biological Evaluation: Top Big mistakes

0 secs; February 13, 2023

Medical Device News: February 2023 Regulatory Update

0 secs; February 06, 2023

How to do Post-Marketing Surveillance in the US (vs EU)?

0 secs; January 30, 2023

How to evaluate Benefit-Risk Ratio for Medical Devices?

0 secs; January 23, 2023

Breaking News: EU MDR Extension Proposal is out for consultation

0 secs; January 16, 2023

How to improve the relationship between QA – RA and Marketing?

0 secs; January 09, 2023

Medical Device News: January 2023 Regulatory Update

0 secs; January 03, 2023

Grow your LinkedIn Profile with Karandeep Badwal

0 secs; December 26, 2022

Is EU MDR extended? with Erik Vollebregt

0 secs; December 19, 2022

MDCG, Team-NB, BVMed & Team-PRRC tell you all about PRRC

0 secs; December 12, 2022

Medical Device News – December 2022 Regulatory Update

0 secs; December 06, 2022

How to choose the best Sterilization Method for Medical Devices?

0 secs; November 28, 2022

Why Risk Management is important to Medical Device development?

0 secs; November 21, 2022

Regulatory Pathway: How to reach the US market? [510k exempt]

0 secs; November 14, 2022

Your Software/IVD clinical report is completely WRONG!

0 secs; November 07, 2022

Medical Device News – November 2022 Regulatory Update

0 secs; October 31, 2022

Can you go to Jail as a PRRC? [Elem Ayne]

0 secs; October 24, 2022

How to be MDSAP certified for your Medical Devices?

0 secs; October 17, 2022

Medical Device News – October 2022 Regulatory Update

0 secs; October 10, 2022

What do Clients, Followers, Team, … think of Easy Medical Device?

0 secs; October 03, 2022

How to select your Notified Body and understand the full process?

0 secs; September 26, 2022

How to become the best PRRC ever? [Ronald Boumans]

0 secs; September 19, 2022

Why do you need an Initial Importer for the US Market?

0 secs; September 12, 2022

Medical Device News: September 2022 Regulatory Update

0 secs; September 05, 2022

SaMD or SiMD – How to create your Design Dossier?

0 secs; August 29, 2022

New Blue Guide – What is the impact on Medical Devices?

0 secs; August 22, 2022

Why are we not Discontinuing your Products?

0 secs; August 15, 2022

When you think “510k” but FDA says “DeNovo” with Spencer Jones

0 secs; August 08, 2022

How to create your Technical Documentation? [EU MDR and IVDR]

0 secs; August 01, 2022

Maybe you need a Cleanroom? Let’s check with Philippe Bourbon

0 secs; July 25, 2022

AI Act vs EU MDR 2017/745 are they compatible? [Erik Vollebregt]

0 secs; July 18, 2022

Medtech Europe Forum interviews (MDR, EUDAMED, CER & MECOMED)

0 secs; July 11, 2022

Medical Device News – July 2022 Regulatory Update

0 secs; July 04, 2022

Attention! 1 year before UKCA is the law for Medical Devices in the UK

0 secs; June 27, 2022

Why is it great for Importers to be ISO 13485 certified? [Cristina Miroescu]

0 secs; June 20, 2022

What are some Quality Common Mistakes? [Karandeep Badwal]

0 secs; June 13, 2022

Medical Device News: June 2022 Regulatory Update

0 secs; June 06, 2022

Let’s introduce you to our eQMS SmartEye with Anindya Mookerjea

0 secs; May 30, 2022

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