We have established independent companies in many of the markets listed below to act as your local authorized representative and compliance agent in the medical device market.
Partner with us to streamline your market access and regulatory compliance efforts, minimizing the risk of application rejections and reducing unnecessary costs.
Regulatory Strategy and Roadmap
Technical Documents Compilation, Submission, and Management
Post-Market Surveillance and Vigilance Solutions
Seamlessly integrate a global market access regulatory partner into your operational workflow, enhancing compliance and market entry efficiency.
We assist you with identifying which markets to expand to leveraging existing registrations and approvals.
Our local regulatory experts provide strategic support to determine classification of your product portfolio and the number of registrations that are required.
Based on the classification of your products, we can outline the required steps and information to obtain your registration.
Whether looking for more information or ready to partner with us, we're here to guide you through every step of the regulatory process.