From years of experience, we know what medical device manufacturers/distributors want: reliable advice with flexibility, transparency, fast and low costs to get NMPA approvals for their products.
All our advisors are from global leading medical technology providers, with different kinds of medical device regulatory affairs experience, this will assure the long-term success of our clients and our team. With our creative cloud-based system, our clients can easily track and manage their projects, fully compliance with NMPA regulations from the very beginning, the design input stage, as well as the whole life-cycle of the medical devices.
Unhappy With Your Current Project Progress?
We continually meet people who have the discipline to plan and process for the registration of their products, but they have been let down by the advice they have received. Whether it’s because of poor performance or bad management, we might be able to help you improve your situation.
Our team members have extensive experience helping our clients restructure their strategy to ensure their project is going in the right way. And our Cloud-based system can provide a creative and efficient way for regulatory affairs.
We have a group of RA professionals throughout China committed to assisting medical device manufacturers or distributors across the world to get their products approved in China. If you are looking for help with your regulatory planning, then get in touch with us today.