With our clinical trial workflow and data management software we want to make a contribution to the efficient conduct of science based clinical research in compliance with regulatory requirements all over the world.

Professionals involved in clinical research operate in a challenging and complex environment, with increasingly demanding rules and regulations.

We at Promasys think that clinical trial software solutions should support those professionals to focus on doing what they are good at. It should not burden them with the need to learn how to program. Or make them dependent on internal or external programmers, or expensive consultants.

Good clinical trial software is about empowerment. It should allow the clinical trial professionals to perform their tasks efficiently and effectively. And it should solve their quality assurance and regulatory compliance needs.

This has been the main thread throughout the development of our Promasys software, since the start in 1988. It still is today.

Everyday, we make it our mission to provide researchers and research organizations with tools to efficently conduct quality controlled clinical research, without programming and/or support from IT personnel.