Technical Documentation per EU MDR is built as per annex II and annex III. Now you can create the technical documentation in very easy manner. The post We help you under EU Technical Documentation appeared first on Medical Device Regulation and ISO quality standard ..read more

You need an eQMS but why. Let me tell you on this article why this is important and let me also help you on that. Contact us at the end if you are needing support. The post eQMS: Streamlining ISO 13485 Compliance & Registration appeared first on Medical Device Regulation and ISO quality standard ..read more

Maybe you are thinking of building a cleanroom for your Medical Device industry. Then read that first to have a clear understanding of how much this cost and also all the maintenance to perform. The post How to set up a Cleanroom for your Medical Device Industry? appeared first on Medical Device Regulation and ISO quality standard ..read more

Placing a devicec in the EU, UK and Switzerland can start to be complicated with what is happening in the region with Brexit, Swixit and the issuance of new legislations. Let's look at that. The post How to place Medical Devices in the EU, Switzerland & the UK? appeared first on Medical Device Regulation and ISO quality standard ..read more

Internal audit is a tool that is available within ISO 13485 or QSR 21 CFR part 820. We will explain how to perform it the right way The post How to perform your Internal Audit the right way? [ISO & QSR] appeared first on Medical Device Regulation and ISO quality standard ..read more

IVDR is the new In-Vitro Diagnostic Regulation for the European Union. So what should you expect from it? How can you be ready? What are the elements to take care of? I will tell you everything on this podcast. The post How to survive IVDR after 26 May 2022? [IVDR 2017/746] appeared first on Medical Device Regulation and ISO quality standard ..read more

This is a good question. Should we first focus on documents creation or should we focus on our prototypes. This is something that we discuss on this article. The post Should you start with Product Development or Document Creation? appeared first on Medical Device Regulation and ISO quality standard ..read more

A Software as a Medical Device (SaMD) is really a specific kind of medical device. I teach you on this article all that you need to follow to put it on the market. I developed a 3 step program to put any medical device on the market. The Route Plan. You need to plan all before to start your journey. Follow the Medical Device Regulation MDR 2017/745 that should be in place before 25 May 2020. The post What is Software as a Medical Device? (SaMD) – Rule 11 MDR 2017/745 appeared first on Medical Device Regulation and ISO quality standard ..read more

The label is an integral part of the Medical Device, So having a non-compliant label is like having a bad medical device on the market. The post How to Create a Label as per EU MDR 2017/745? appeared first on Medical Device Regulation and ISO quality standard ..read more

Technical Documentation per EU MDR is built as per annex II and annex III. Now you can create the technical documentation in very easy manner. The post We help you under EU Technical Documentation appeared first on Medical Device Regulation and ISO quality standard ..read more