Clinical Informatics
The medical informatics field is going through rapid change. Advances in medicine combined with new technologies are revolutionizing the way medicine is practiced. With modern molecular biology technologies, it is possible to probe and understand the genetic basis of diseases, opening up the possibility of personalized medicine. On the downside, it also unleashes an avalanche of data that cannot be analyzed using traditional methods.
In addition, with clinical informatics comes the progression to patient-centric care, and patient access to a plethora of online information. This combined with an increasingly mobile population spurs the need to develop information technologies that can rapidly store, manage, visualize and integrate biomedical data and patient information - delivering it anywhere in the world.
Persistent Advantage
- Medical experts with in-depth understanding of clinical trials domain
- Experience working with premier cancer research institutes, medical centers and pharmaceutical companies
- In depth understanding of experimental data like tissue, microarray, proteomics and genotyping data
- Expertise in SAS, Oracle Clinical
- In depth understanding of regulatory requirements
- Reusable components for 21CFR Part 11 implementation
- Ready checklist and infrastructure for implementing HIPAA guidelines
- Building modules for making legacy applications HL7 compliant
- caBIG® compliant application development
Persistent Offerings
- Clinical Trial Management Systems (CTMS)
- Automating CTMS business process workflow
- Developing web-based CTMS system components for
- Patient consent process
- User defined CTMS protocol
- Platform for
- Flexible web-based forms for clinical data input
- Configurable querying and reporting tool for monitoring outcomes
- Web-based CTMS for preclinical study management on model animal supporting user defined protocols
- Decision support system for multi-site clinical trial management
- Clinical Data Management Systems ( CDMS)
- Clinical Data Warehouse design for
- Performance management of clinical trials
- Unifying clinical, tissue, genotype data
- Pharmacogenomic analysis
- Ready interfaces available for standard products such as Oracle Clinical, SAS
- Extending CDMS to support clinical, pathological annotations
- Clinical Data Submission and Regulatory Standards
- Development of applications compliant with 21CFR Part 11, HL7, caBIG®
- Ready development environment compliant with HIPPA
cancer Biomedical Informatics Grid, caBIG and the caBIG logo are registered trademarks of HHS used in connection with the National Cancer Institute’s caBIG® program