Clinical Regulatory

arivis started with the first ever cloud-based eDMS system designed for life sciences in 2005. We enhanced these tools with the addition of eCTD Regulatory Submission Management along with full Virtual Data Room capabilities. Now arivis Clireo provides the only Azure based Clinical eTMF and ISF with full eDMS capabilities. And Clireo eMPM supports end-to-end Promotional Materials Management for Medical, Legal, and Regulatory review and approval. Combined with Clireo eCTD and the new Module 1 for the FDA eCTD, Clireo creates the industries only integrated Promotional Materials Management system with integrated eSubmissions capabilities.

Clireo integrates arivis' complete RIM solution for xEVMPD, IDMP, tracking, planning and communication management. 

What we do

A team you can count on
Our industry experience and personal touch provide you with software and service that will meet your needs. Our people know your name and work with you as part of your team.

RIM on-premise or in the cloud
Either our Clireo cloud-based solutions of GlobalTrack enterprise solutions provide exactly the right fit for your organization.

Industry Leading
You'll find our team at speaking at conferences, giving webinars and participating in industry standards bodies. This expertise and access results in better solutions to you.

Support
In the US or in Europe, we are here to support you and your team. Our solutions are provided with multi-channel support options.

Who we are

arivis started with the first ever eDMS system that integrated Business Process Management (BPM). We enhanced these tools with the addition of eCTD Regulatory Submission Management along with full Virtual Data Room capabilities. Later we introduced more regulatory submission management capabilities with support for 510k, PMA, and custom submission types. This enables us to support any and all output required by global Biotech, Pharmaceutical, Diagnostic and Medical Device companies. Now arivis Clireo provides the only Azure based eTMF with full eDMS capabilities. And Clireo eMPM supports end-to-end Promotional Materials Management for Medical, Legal, and Regulatory review and approval. Combined with Clireo Submissions and the new Module 1 for the FDA eCTD, Clireo creates the industries only integrated Promotional Materials Management system with integrated eSubmissions capabilities.

Regardless of your size or the type of Life Science company you are, arivis provides solutions to critical challenges in an increasingly complex industry.

The arivis team is comprised of industry experts with extensive experience in technology and Life Sciences. Click here to learn more about our people.