Medical Device made Easy Podcast

Medboard https://www.medboard.com/   EU   Training   Events MedtechConf events – Check the MAP   ROW Australia Mexico GMP for Mexico – Draft document: https://www.dof.gob.mx/nota_detalle.php?codigo=5734591&fecha=26/07/2024#gsc.tab=0   South Africa   PODCAST […] The post Medical Device News November 2024 Regulatory Update appeared first on Medical...

In this episode, Adam Isaacs Rae will help us shape your Regulatory Compliance Strategy. This is a requirement of the EU MDR and IVDR but it doesn’t provide much information. So let’s review that together. The post What does a strategy for regulatory compliance looks like? appeared first on Medical Device made Easy Podcast . hamza benafqir

In this episode, Georg Digel will help use solve 3 major problems with our CAPAs. He will tell you what these problems within your Quality Management System are and propose some solution. We will also talk about the education of the team. The post What are the TOP 3 issues on CAPAs?  appeared first on Medical Device made Easy Podcast . hamza benafqir

Medboard: https://www.medboard.com/ EUROPE EVENTS NB ROW Middle East Northern America South America: PODCAST Social Media to follow The post Medical Device News, October 2024 Regulatory Update appeared first on Medical Device made Easy Podcast . hamza benafqir

In this episode, Lucas Pianegonda will help us to select the right material for your medical device and answer questions that you maybe would love to hear his answer. We will also talk about sustainability for plastics. So, check this. The post How to select the best plastic for your Medical Device? appeared first on Medical Device made Easy Podcast . hamza benafqir

In this episode, Claire Dyson will give us the recipe to launch correctly your Medical Device when you go abroad and for that we will take the example of EU and US. The post UK vs EU vs US – How to switch to another region easily?  appeared first on Medical Device made Easy Podcast . hamza benafqir

In this episode, Cesare Magri will try to improve our skills on PMCF literature search. We will investigate on the misconceptions and what people should make to do it right. The post How to do a PMCF Literature Search for Medical Devices?  appeared first on Medical Device made Easy Podcast . hamza benafqir

EU Switzerland Training Events: ROW Medical Device Live Expert: Podcast The post Medical Device News, Septembre 2024 Regulatory Update appeared first on Medical Device made Easy Podcast . hamza benafqir

n this episode, Martin King will share with us his practice of AI in the context of Quality and Regulatory affairs for medical devices. This will explain to you some best practices to maintain to avoid some pitfalls. The post How to use AI GPT for your Quality and Regulatory work? appeared first on Medical Device made Easy Podcast . hamza benafqir

In this episode, Stephen O’Rourke that was not working within the Medical Device industry will share with us is journey from Zero knowledge in the field to running projects. Listen to his journey in case you are also willing to breakthrough the medical device field. The post How to go from Zero to Hero in Medical Devices? appeared first on Medical Device made Easy Podcast . hamza benafqir

: In this episode, I have invited Ralf Gansel to help us understand the process for Certification of your product and what is the lifecycle for it. We’ll discuss about Transfer or certificates, or notification of changes or why there is a renewal and not continuous surveillance… The post Manage the Transfer/Renewal/Surveillance/Change of your CE certificate appeared first on Medical Device made Ea...

In this episode, Beat Keller will help you understand Harmonized Standards and how to use them and also how to do when there is no Harmonized Standards. So stay tuned. The post How to use Harmonized Standards for Medical Devices? appeared first on Medical Device made Easy Podcast . hamza benafqir

TÜV SÜD is one of the main notified bodies. And they are celebrating their 100th Class D certificate. Andreas Stange will explain to us what they learned and how manufacturers can improve their certification process. The post IVDR Class D – Lesson learned from Notified Bodies appeared first on Medical Device made Easy Podcast . hamza benafqir

The EU MDR is in constant update and this change on the interruption of supply of medical devices should be integrated. The post EU MDR Major update: Interruption or Discontinuation of supply! appeared first on Medical Device made Easy Podcast . hamza benafqir

How to register your Medical Devices in the UAE with Ahmed Hendawy from Registitute and Monir El Azzouzi from Easy Medical Device The post How to register your Medical Device in the UAE? appeared first on Medical Device made Easy Podcast . hamza benafqir

Medical Devices should follow regulations like EU MDR or IVDR but also some regulations that are also targeting some components like batteries. So for that there is EU Battery Regulation 2023/1542. Erik Vollebregt from Axon Lawyers will explain the impact of the regulation to your product. The post EU Battery Regulation – How to be ready?  appeared first on Medical Device made Easy Podcast . hamza...

The AI Act will be soon officially published even if we know the text will not change. So let’s help you to be prepared for its implementation. Fabien Roy will explain the challenges that he has recognized. The post AI Act – What are the challenges for Medical Devices?  appeared first on Medical Device made Easy Podcast . hamza benafqir

Medboard EU UK Swiss MEDTECH CONF LIVE SESSION US Australia Saudi Arabia Malaysia South Africa PODCAST Social Media to follow The post Medical Device News, July 2024 Regulatory Update appeared first on Medical Device made Easy Podcast . hamza benafqir

As a Software developer, we need to understand what a Regulator can look at when you submit an AI/ML Model. Let’s listen to Richie Christian from Wega The post How to submit your AI/ML SAMD the right way? appeared first on Medical Device made Easy Podcast . hamza benafqir

The Notified Body is an important actor for Medical Devices that seek a CE certification under EU MDR and IVDR. In this Episode Thomas Lommatzsch from AFNOR will explain to us the difficult process of designation. The post AFNOR – How is a Notified Body designated?  appeared first on Medical Device made Easy Podcast . hamza benafqir

If you are working within Surgical Instruments, or any products that need to be really clean prior to be sent, then this episode is for you. We discuss with Heena Thakkar what is the best way to manage cleaning validation. The post Cleaning Validation – How to select the worst case?  appeared first on Medical Device made Easy Podcast . hamza benafqir

The post Medical Device News June 2024 Regulatory Update appeared first on Medical Device made Easy Podcast . hamza benafqir

In this episode, Amandine Broussier will share with us her expertise on Usability with a specific scope on the summative evaluation. The objective will be to share with you some of the common mistakes done by the industry. The post Summative Evaluation – Common mistakes  appeared first on Medical Device made Easy Podcast . hamza benafqir

Sometimes, you want to manufacture a product, but you don’t have the capacity or even the infrastructure. Then why not asking a Contract Manufacturer to do that for you. Let’s explain to you that you should take care of when working with one. The post Are you more Corrections or Corrective Actions or Preventive Actions? appeared first on Medical Device made Easy Podcast . hamza benafqir

Sometimes, you want to manufacture a product but you don’t have the capacity or even the infrastructure. Then why not asking a Contract Manufacturer to do that for you. Let’s explain to you what you should take care of when working with one. The post How to select and evaluate your Contract Manufacturer?  appeared first on Medical Device made Easy Podcast . hamza benafqir