Following the release of Promasys version 6.0 in December of last year –which brought exiting new features like the eCRF, coding for adverse events and conmeds, and a new streamlined subject enlistment procedure– we are about to launch the next new version that will bring great benefits to Promasys users.

Presently, final release testing is being conducted, and the formal release of version 6.1 is scheduled for the end of September.
Version 6.1 will come with some important new features: the WebCRF, Promasys' browser based EDC system, and electronic signatures.

In March of this year, we installed our software in the National Center of Neurology and Psychiatry in Tokyo, Japan. The installation was followed by a 2 day intensive training course. Our Tokyo based support staff continues to help the NCNP getting quickly up and running.

"The Clinical Research Unit of the NCNP Hospital is involved in conducting clinical trials of newly developed drugs. Two adviser doctors and 15 clinical research coordinators (CRCs) including 3 full-time staffs (1 pharmacist and 2 nurses) work with the doctors to evaluate the safety and effectiveness of new drugs, paying close attention to patients' privacy and safety, as well as their human rights."

In July of this year, Promasys BV signed a contract with the University Clinical Center Heidelberg, of the Department of Clinical Pharmacology and Pharmacoepidemiology, Faculty of Medicine of Heidelberg University.

The center belongs to the most prestigious and active clinical research centers in Germany. Implementation (installation, validation, training) of our Promasys system in the University Clinical Center Heidelberg is scheduled to start in September of this year.

Now you can run your clinical trials and manage your data in compliance with international standards and regulations. Set up new trials without doing any programming. Improve the efficiency of your organization. And become more cost effective.

Promasys^® offers researchers and research organizations a tool for streamlining clinical trials. It provides the infrastructure for high-quality scientific research. The software architecture of Promasys, the extensive multi-center support and the detailed configurability of access rights make Promasys the ideal platform for clinical trial networks and multi-center studies. Click here to view the key features of Promasys.

Promasys has extensively proved its applicability in the field. Over a period of more than 20 years, the program has been developed and tested in a demanding clinical research environment. Promasys has demonstrated its strength in hundreds of clinical trials. To date, more than 300 trials managed in Promasys have resulted in publications in international scientific journals, with a growing number of (academic) hospitals and CROs using the software. Click on the following link to download the Promasys Introductory Presentation in PDF format.