Web-based Clinical Trial Portal and Study Communication Centre

With secured role-based access for all Parties involved in a Clinical Trial or Research project. Clinical Study-Portal has been built from the ground to be attractive and as user-friendly as possible.
Thumbnail of Clinical Investigator PortalIt is fully customizable and has been developed in close cooperation with both Bio-Pharmaceuticals, CRO’s and Clinical Investigators. Because of this approach, Study-Portal features an intuitive and engaging user experience. Our software allows for people who participate in a clinical study or trial to connect to each other and share information, knowledge and experience.
Clinical Study-Portal is a generic solution, able to handle and share information on multiple Clinical Trials. Read More

Key Features

Sharing Clinical Trial Documents

Clinical Trial Documents

Documents are a major cornerstone of Trials. Clinical Study-Portal will help you organizing your Documents and make sure everybody is working with the latest version. Role-based settings dictate which documents a user is allowed to view. Clinical Study-Portal also handles Trial Master Files (eTMF), Images (e.g. X-Rays) and Videos (e.g. Site Training videos). Read more

Clinical Trial CommunicationClinical DBMS Interface

Clinical Study-Portal can interface with your Clinical DBMS and will keep all Stakeholders up-to-date by presenting your key study information in its web-based environment.
User authorization and role settings govern the specific content any user will be able to see. Read more

Clinical Trial CommunicationBlog, News and Communications

Enhance interaction and communication between Bio-Pharmaceutical employees, CROs, Clinical Investigators and Patients by Role-driven access to Blog, News items and Communication Center.
This can be a very powerful tool to enhance patient motivation in your clinical trial, resulting in lower drop-out rates. Read more

Clinical Investigator Profile

Profiles of Clinical Trial Participants

“Who is responsible for .. in this trial?” This is the number #1 question of Site personnel and can easily be answered by including a Profile section in your Clinical Investigator Portal.
The Profile is fully configurable,you can decide on the actual Profile content. Different content can be set for different Groups of Users.
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Co-design Partners

New modules and enhancements are designed in close cooperation with clients.This benefits the client as they will find many items from their wish-list in the Portal. And it allows us to maintain a high usability standard.

Currently, we are highly interested in new co-design partners who want to use the Portal technology to interact with study Subjects (e.g. patients). We strongly believe that better patient participation results in higher accrual rates and lower drop-out rates.

Your initial participation as co-design partner is off course free of charge.
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