About Global regulatory press
Global Regulatory Press: Your Trusted Partner in Medical Device Regulatory Affairs
Global Regulatory Press is a leading publisher of the Journal of Medical Device Regulation and other e-books on medical device regulatory affairs. With over 20 years of experience in the industry, we have established ourselves as a trusted partner for companies seeking to navigate the complex world of medical device regulation.
Our mission is to provide our clients with accurate, up-to-date information on regulatory requirements and best practices, enabling them to bring safe and effective medical devices to market quickly and efficiently. We understand that navigating the regulatory landscape can be challenging, which is why we offer a range of services designed to support our clients at every stage of the process.
Journal of Medical Device Regulation
The Journal of Medical Device Regulation (JMDR) is our flagship publication, providing expert analysis and commentary on global regulatory developments affecting medical devices. Published quarterly, JMDR covers topics such as pre-market approval processes, post-market surveillance requirements, quality management systems, clinical trials and more.
Our team of experienced writers includes leading experts in the field who are dedicated to providing insightful analysis that helps readers stay ahead of changing regulations. Whether you are a manufacturer looking to bring a new product to market or an industry professional seeking insights into emerging trends and best practices, JMDR has something for you.
E-Books on Medical Device Regulatory Affairs
In addition to JMDR, Global Regulatory Press offers a range of e-books covering various aspects of medical device regulation. Our e-books are written by subject matter experts with extensive experience in their respective fields. Topics covered include:
- EU MDR/IVDR
- FDA regulations
- Clinical evaluation reports
- Post-market surveillance
- Quality management systems
- And more
Our e-books are available for purchase through our website or through major online retailers such as Amazon.com. They provide valuable insights into key issues affecting medical device manufacturers today and offer practical guidance on how to navigate the regulatory landscape.
Consulting Services
In addition to our publications, Global Regulatory Press offers consulting services designed to help companies navigate the regulatory landscape. Our team of experts can provide guidance on a range of issues, including:
- Regulatory strategy development
- Pre-market approval processes
- Post-market surveillance requirements
- Quality management systems
- Clinical trial design and execution
We understand that every company is unique, which is why we tailor our consulting services to meet the specific needs of each client. Whether you are a small start-up or a large multinational corporation, we have the expertise and experience necessary to help you achieve your regulatory goals.
Conclusion
At Global Regulatory Press, we are committed to providing our clients with accurate, up-to-date information on medical device regulation. Whether you are looking for insights into emerging trends and best practices or need guidance on navigating complex regulatory requirements, we have the expertise and experience necessary to help you succeed. Contact us today to learn more about how we can support your business.