We need " Clinical Trial Portal".
Clinical Study-Portal should be designed to enable Information sharing with all relevant parties in Clinical Studies. Clinical Study-Portal should be built from the ground to be as attractive and as user-friendly.
It should be developed in close cooperation with both Bio-Pharmaceuticals, CRO’s and Clinical Investigators. This portal need to allow 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.
Some Key Features: 1. Clinical Trial Documents: 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).
2. Clinical DBMS Interface: 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.
3. Blog, 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.
4. Site/Investigator Profiles: The User (eg. Investigator) Profile is fully configurable,you can decide on the actual Profile content. Different content can be set for different Groups of Users.
Please send your proposal along with detailed modules and commercials.
Time frame should be two months.