#iso

#55 Standardi Podcast

Prawo - pomaga czy przeszkadza chronić środowisko? Rozmowa z Martą Banasiak

Intro Crónicas Fotográficas

Cyfrowe pieniądze zamiast gotówki. R. Górski (ISO): DAJCIE LUDZIOM WYBÓR!

Ep10: Veicoli elettrici vs Acqua

Czułość ISO w aparacie fotograficznym (S01E34)

Podstawy fotografii (S01E16)

Innovación de servicio: Desafíos y consejos para pequeñas y medianas empresas

Ep. 11 - Come implementare i sistemi di gestione?

Ep.227 w/ Ivan Lovegren "Building a trustworthy hobby marketplace"

Hablando de innovación: José Orlando Montes comparte sus experiencias y conocimientos

Capitulo 7. Desafíos comunes en la implementación de acciones correctivas

ISO 9001. Capitulo 2. Explorando los principios de calidad: Liderazgo, enfoque en el cliente y involucramiento del personal.

34. La compliance come asset - con Vittorio Campione

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