INNOVATION AND SIMPLICITY WITH TENTO+

Medical Device Regulatory Compliance Software

Tento+ is one of the leading names in medical device regulatory compliance software, powered by AND Technology Research, a trusted name with more than 40 years of experience in design and development in regulated markets. AND Technology Research offers a unique depth of understanding within the medical device industry and its complex regulatory landscape.

The innovation of Tento+ brings an unprecedented simplicity to medical device regulatory compliance software that has been built specifically to serve the needs of product development teams.

TENTO+ SOLUTION

Ensure compliance with regulatory software

Employing the right medical device regulatory compliance software is an essential step in helping you ensure the successful approval for your medical device. Powered by AND Technology Research, a trusted name with more than 40 years of experience in design and development in regulated markets, Tento+ is the result of our dedication to providing a disruptive digital approach to compliance.

With a firsthand understanding of the challenges faced by businesses in navigating regulatory requirements, Tento+ is designed to empower product development teams with clearly defined processes to efficiently deliver a collaborative and up to date working environment.

Assure Compliance success with Tento+

If you are looking to meet regulatory standards for your medical device, Tento+ is the new way to take the complication out of your journey to compliance.

Simply check the appropriate keywords relevant to your device and Tento+ will instantly create an individualised checklist for your product’s regulatory requirements. Tento+ will then allow you and your team to manage activities, record testing results and track progress. To try our free Tento+ demo, simply complete the form.