Formly streamlines EU medical device certification, ensuring rapid CE marking with automated documentation and expert guidance.
Formly is an innovative AI-driven platform designed to simplify the medical device certification journey in the EU. It accelerates the CE marking process by offering automated, MDR-compliant documentation and expert regulatory support. Users can generate necessary documentation efficiently by simply answering straightforward questions, significantly reducing the time and complexity involved in satisfying regulatory requirements. With features tailored to assist companies navigating the intricacies of medical device regulations, Formly empowers users to focus on their product development while ensuring compliance.
A CE mark indicates that a product complies with EU safety and health regulations, allowing it to be marketed within the EU. It is essential for legal market access and consumer confidence.
The time to receive a CE mark can vary, but with Formly's automated processes, it can be significantly reduced. Typically, it ranges from several weeks to a few months, depending on the complexity of the device.
Absolutely! Formly is designed to guide users through the certification process, making it accessible even for those without prior knowledge of medical device regulations.
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