Global regulatory information brought together into one location for all the Medical Device Solutions you will need to be successful.
At MedDev Global, we intend to provide you a broad range of topics and resources in order to help you successfully navigate the Medical Device Regulatory Environment. Our forums allow you to freely collaborate by asking questions and helping others regarding the areas of 21 CFR guidance, specific 510k guidance, and general / global medical device information. The Global Regulatory Environment is constantly changing, and you need to be aware of all the requirements in order to effectively gain market entry into desired countries. Sometimes you will need direct help, and if so, please visit Our Services and the Resources tabs for additional support to help you succeed. Information will soon be available in these areas.
This portal is intended to support the following professionals:
- Research and Development
- Project Managers
- Legal Services
- Any medical device business professional
Whether your organization is small or large, and no matter your location globally, the information here can help you. We are dedicated to becoming the top destination for Global Regulatory Intelligence and will work hard to satisfy the needs of you, the Medical Device Community. Check back soon for the go-live of the Global Regulatory Intelligence Portal™ also known as GRIP™.
We encourage and welcome your feedback to help us make this portal better for you. Please feel free to contact us below.
Finally, the more professionals that use this site, the more resourceful it will become as a one-stop source for all your needs. Spread the word to help this portal grow.
This site is currently under active construction to make its full features soon available, however, the forums have been launched at this time. Become a member and begin collaborating!