Clinical Trial Portal and Study Communication Centre
Clinical Study-Portal has been designed to enable Information sharing with all relevant parties in Clinical Studies. Clinical Study-Portal has been built from the ground to be as attractive and as user-friendly as possible. Therefore, it is an ideal tool to for enhancing Sites and Subject engagement.
It 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 documents, information, knowledge and experience.
Clinical Study-Portal is a generic solution, able to handle and share information on multiple Clinical Trials. Read More
Role-based settings dictate which documents a user is allowed to view or update. Clinical Study-Portal handles Trial Master Files (eTMF), Images (e.g. X-Rays) and Videos (e.g. Site Training videos).
Clinical Study-Portal will keep all Stakeholders up-to-date by presenting your key study information in its web-based environment.
User authorization govern the specific content any user will be able to see.
Enhance interaction and communication between Bio-Pharmaceutical employees, CROs, Clinical Investigators and Patients by Role-driven access to Blog, News items and Communication Center.
6th Dutch National Trial Conference, Amsterdam (Netherlands), Jun. 21
The major theme of this year’s meeting is how to ‘market’ Dutch Trials.
Visit our booth and see how Study-Portal can assist you in ‘marketing’ your trials.
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.