🔍 *Verify Before You Submit!* ✅ As part of the *global harmonisation of medical device regulations* , many regulatory authorities are working closely with third-party service providers to streamline device approvals and market placement. 🌍 These collaborative systems aim to simplify international compliance—but many of these frameworks are still in development. Meanwhile, alternative platforms or services claiming full compliance are already operating, yet they are not officially licensed nor do they share their compliance status with national regulators. 🚨 Before you submit any regulatory documentation, always verify the licensing and authorization status of the service provider with your national regulatory authority. This step is critical to: * Avoid non-compliant submissions ❌ * Prevent costly delays 🕒 * Ensure successful market access for your device ✅ 👉 Stay informed. Stay compliant. Always verify. https://www.regulatorymedicaldevice.com/