Starting December 28, 2024, the Directive (EU) 2022/2380 will require a USB-C charging interface for a range of electronic devices sold in the European Union. This regulation is part of a broader push to simplify charging for consumers while reducing electronic waste across the EU. But how will this impact manufacturers, and what do they …
EU Common Charger Mandate Starts December 2024: What to Know Read More »
Before you read a NOTE: For more detailed information on the new cybersecurity regulations and how they might impact your devices, check out also our comprehensive guides: –Get Ready fo the 2025 EU cybersecurity regulations; – Does you IoT Equipment need to comply with the New EU cybersecurity regulations. On August 1, 2025, the European Union will …
Understanding the 2025 Cybersecurity Regulations for EU Compliance Read More »
CellAED achieves CE certification. Wireless and Medical come together in CellAED. A great teamwork between all partners. “We have done it!”. IoT Consulting partners is proud to be part of the realisation of this life changing product and being a part of making Rapid Response Revival (RRR) dream come true: “Realising CellAED achieves CE certification”. …
Why do I need an Authorised Representative when placing my product on the European (and/or UK) market? And why should I especially consider appointing one from July 16th 2021? What impact will the new product market surveillance legislation have on me? As in the European Union Regulation 2019/1020/EU comes into force, a lot will change …
The healthcare industry is undergoing a significant transformation driven by the Internet of Things (IoT). MEDTECH is evolving, increasing usability and accessibility, while the demand for home-use health applications continues to rise, especially in light of the COVID-19 pandemic, which necessitated social distancing and remote care solutions. The past year has highlighted the growing benefits …
The Rise of IoT in Healthcare: A MEDTECH Evolution Read More »
Let us talk about the correct way of placing the Notified Body behind the CE logo, why size matters? Let us get to the answers first, followed by the explanation. Notified body labelling how it should not be. During my work for a Certification body, many questions from manufacturers have passed, initially appointed for the …
What steps do you need to take to become a successful startup in IoT (Internet of Things)? Now let us get one thing clear, if we would be able to find a complete book guiding and guaranteeing us from A to Z, then why would we still look for this article? To become and being …
Integrating RF modules into IoT products isn’t as simple as plugging in a certified module. The REDCA TGN 01 document provides essential guidance for manufacturers, emphasizing that both the RF module and the final product must undergo compliance testing. Even if your module is pre-certified, it doesn’t mean your product is automatically compliant. This document …
What is the UKCA marking? UKCA stands for UK Conformity Assessed. The end of 2020 is nearby. The UK will leave the EU, and on December 31st, 2020, the transition period will come to an end. For a long time, there have been questioning marks what will happen to the Conformity Assessment routes to follow …
What is the UKCA marking and from when is it applicable? Read More »
With the 2014/53/EU Compliance Test Plan, you will know from phase 1 of your product design what is required for product compliance. Compliance with the essential requirements and the availability of the TCF is a big part of the directive; however, it will not end there. You want to conquer the world with your unique …
Iot Consulting Partners 2014/53/EU Compliance Test Plan Read More »
