Registry Indonesia
Overview
Registry, hereinafter referred to as RegINA (Registry Indonesia), is an organized system that collects uniform data (clinical, demographic, behavioral etc.) related to the samples in its biobank. RegINA will in due course also connect this information with information generated from research activities on the samples stored in the biobank, including genomics information. Data curated by this system will be made accessible by researchers who wish to evaluate specific disease outcomes for a population of interest.
Business Scheme
Each Hub within BGSi's network will be able to utilize the data managed through the RegINA (BGSi registry system) to drive evidence-based decisions, and share best practices. In addition, all clinicians use RegINA data as the foundation for registry-enhanced or registry-based research, clinical trials, or post-market surveillance studies.
Access to the information by researchers outside of the Hubs will be managed by BGSi and will require the submission of a detailed protocol for evaluation by BGSi and its Hubs.
RegINA emphasizes the importance of:
Accessible and interoperable data
General clinical data repository
Integration clinical data repository
Low-cost registry and hubs expansion
Evolving healthcare IT
Data security and privacy
