The Journal of Medical Device Regulation (JMDR) is read and referenced by regulatory affairs, quality assurance, clinical, and compliance professionals across the global medical device and IVD industries. Our readers include regulatory leaders from manufacturers, industry associations, Notified Bodies, consultancies, law firms, and healthcare technology organisations worldwide.
The testimonials featured below highlight the Journal’s value in supporting regulatory intelligence, compliance, post-market surveillance, and international market access activities.
"The JMDR is a valuable journal for everyone working in the global regulatory landscape for medical devices. It covers topics from all over the world and from quality topics to regulatory processes and topics from end to end. Not only medical device regulation but also horizontal topics like AI and data, cybersecurity and many more."
"The JMDR is one of the top publications for regulatory affairs professionals. It has been the go-to source of medical devices regulatory news and analysis for many years, and it helped me throughout my career to stay informed and to learn from other regulatory experts. Whether you need a quick overview of what's new in the medical device regulations worldwide, or an in-depth analysis of a particular topic, JMDR delivers every time. I cannot think of a better value for money for regulatory professionals to continuously learn and stay informed."
"I learned a lot from your publication last year and it was very helpful in keeping me up to date. Looking forward to the next issue and everyone having access."
"As the Italian national association for medical devices and IVDs, we support around 400 companies in regulatory compliance, and over the years JMDR has proved to be an exceptional tool and source of information in doing that. In complex times like these, we have been able to provide a great deal of support to our members thanks to the regulatory news and analysis, especially considering the MDR/IVDR approaching, the pandemic and Brexit to mention a few. I strongly recommend this journal also to companies willing to reach out to new markets: the worldwide countries regulatory analyses are very useful and punctual."
"AccuVein continues to sell very well around the world and your journal continues to be an excellent source of international regulatory information. It seems like nothing ever stays stable in regulatory affairs and yet with your journal in hand I feel I have a partner helping me understand the arcane rules and looking out for surprise changes."
"A few years ago, in 2010, we were looking for ways to improve the efficiency and reliability of our regulatory watch. It was on this occasion that we subscribed to the Journal of Medical Device Regulation (JMDR). Since then, we refer to this publication as we are satisfied with its content and exhaustiveness, even if we are not directly concerned with all the subjects covered."
"Thank you for an excellent Journal, always full of important news regarding new regulations."
"The JMDR helps me being aware of any regulatory changes that could affect our business. It's my starting point for further research and I also rely on it to keep up to date with topical issues in the device community."
"The Journal is very useful to keep up to date with what is going on in the industry. It gives perspective on important issues and I appreciate the international scope."
"JMDR is a rich source of authoritative and up to date regulatory intelligence which is an important resource for us and our clients."
"The JMDR is a great resource of regulatory information. I love the combination of in-depth analyses and short 'Telex' updates from all around the globe."
"Journal of Medical Device Regulation is a good journal to keep up with the latest regulatory news concerning medical devices. The focused articles in this journal wrap up the pertinent information on the changes in regulations. Journal of Medical Device Regulation is a good source for our post-market surveillance activities."
"Thank you for an outstanding, well researched journal. It provides detailed information about regulations, directives and all topics related to medical device approvals worldwide. It is always up to date and helps with regulatory works."
"Our team for regulatory affairs has used your journal for many years as an excellent source of information regarding upcoming regulations and legal changes. The articles and information in the journal are very well researched and written. It is an essential tool for our literary research. We can recommend this journal to anyone who works in the field of regulatory affairs and needs to stay abreast of most recent developments in the EU and worldwide."
