#mdr

SERVICIO GLOBAL DE SEGURIDAD GESTIONADA PARA PREVENIR CIBERATAQUES

How to accelerate your Laboratory Test Results? [Christoph Lindner]

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

Your Software/IVD clinical report is completely WRONG!

What are the surprises during MDR & IVDR transition? [Erik Vollebregt]

Why Design History File (DHF) is so important? [Alexandros Savvidis]

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

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

Why Risk Management is important to Medical Device development?

Biological Evaluation: Top Big mistakes

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

Is EU MDR extended? with Erik Vollebregt

Which devices cannot be Custom-made? [Erik Vollebregt]

Let’s unleash “MDR Classification surprises” [MDR 2017/745]

Medical Device News – January 2022 [Happy New Year]

Medical Device News: December 2021 Regulatory Update

How to evaluate Benefit-Risk Ratio for Medical Devices?

The Step-by-Step recipe to get MDR & IVDR Certified

Is it possible to Private Label a Medical Device under MDR & IVDR?

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

What happened in 2021? Summary for the Medical Device Industry

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

Medical Device News: September 2022 Regulatory Update

How does the EU Commission plan to save IVDR 2017/746?

What are some Quality Common Mistakes? [Karandeep Badwal]

Medical Device News – July 2022 Regulatory Update

How to certify your Software as a Medical Device? (SaMD)

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

Grow your LinkedIn Profile with Karandeep Badwal

How to be MDSAP certified for your Medical Devices?

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

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

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

Medical Device News: February 2023 Regulatory Update

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

Is it a good idea to sue my Notified Body? [Erik Vollebregt]

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

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

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

Medical Device News – December 2022 Regulatory Update

How to choose the best Sterilization Method for Medical Devices?

What lesson did we learn doing Clinical Evaluations? [Cesare Magri]

Why do we need the Common Specification for Class D IVDR?

How to sell Medical Devices online in the EU and US?

Medical Device News: June 2022 Regulatory Update

Medical Device News – November 2021 latest update

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

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

MDCG 2021-27 Placing on the market & Re-labelling with Erik Vollebregt

Medical Device News – November 2022 Regulatory Update