This free tool is designed for medical device companies to provide guidance when transitioning to MDR EU2017/745 through an easy-to-use proven method for understanding, assessing and executing the necessary changes for compliance.
These free tools have been developed by our partners at Regulatory Globe and MedBoard Company Ltd. If you're interested in downloading the full paid version, click here.
Health is one of the basic needs of humans and should always come first. People who cannot cover these basic needs are usually dependent on outside help and that is precisely the goal of the medical technology industry. To develop medical products that improve quality of life and extend life expectancy.
In order to serve this basic need, laws and regulations are inevitable. Regulations ensure safety and quality of products as well as raise the state of the art and thus promote progress steadily. This is why it is important to approach new requirements as an opportunity for improvements, not as a burden. Companies that recognize this will be successful in the long term.
This is where the task of Regulatory Globe begins. Together with our partners, we specialize in monitoring laws and regulations and provide tools that help our clients improve their products and processes, and benefit the people in need of these medical devices. Visit our website to learn more by clicking here.
MedBoard is a MedTech platform and search engine that regularly index, categorize and organize thousands of information and data from all over the world related to Medical Devices and IVDs in the areas of Regulatory, Compliance, Technical, Standards, Commercial and Market data. Covering more than 100 countries, MedBoard tracks and provides all information, including updates, from Authorities, Certification Bodies, Manufacturers, and Suppliers, making any MedTech information accessible, useful, and structured. Visit our website to learn more by clicking here.