Life Sciences and Pharmacy
Transforming data into usable information
Life Science organizations face increasing pressure from tighter government regulations including 21 CFR Part 11 compliance, Good Clinical Practices (GCP), demand for lower prices and safety, and pressure to bring drugs to market faster. Combine this with the load from many manual and paper processes, multiple applications that do not work well together, and the need to work with people at multiple sites, and this creates significant challenges for the clinical trial process and for quickly bringing to market drugs and medical devices.
With Santéon’s proven business process management technology, contract research organizations and life science companies can:
- Tie your disparate systems together in an organized process flow
- Automate your manual paper processes
- Auto-populate your clinical trial related forms
- Follow GCPs and other government mandated regulations
- Speed up your clinical trials to bring drugs to market faster and less expensively
- Coordinate work across multiple trials and sites
- Improve data quality and reduce errors
Transforming the development process
Santéon's innovation leverages & extends your technology
Santéon understands that most life sciences organizations have made significant investments in multiple applications to handle the demands of the drug development process. These applications have been built over time and do not always work well with each other. Santéon's innovative approach helps access data from these different applications in centralized intelligent views without having to disrupt or replace the existing systems. We can also help you create streamlined processes to standardize how this information is efficiently processed. We can work with any data format or system type, including applications such as: clinical data management systems, document management systems, financial reporting systems, protocol management systems, adverse reaction tracking systems, reporting systems, regulatory management systems, etc.
Highlights of some life sciences processes Santéon can address
- Manage compliance of CFR Part 11
- Initiate and manage protocols
- Recruit, pay, and manage participants
- Manage and accelerate clinical trials
- Report to sponsors and communicate with participants
- Process financial billing and tracking
- Manage marketing and sales training
- Manage manufacturing and supply chain
Santéon capabilities to transform life sciences productivity
Santéon can help you help complete your trials faster and more efficiently, increasing the number of trials you complete, driving up revenues and outdoing the competition. Several capabilities of Santéon technology can help your organization increase revenue and efficiency.
- Workflow & automation
- Integration to exchange data across multiple systems in one centralized location
- Intelligent Forms to interact with data from multiple systems
- Business Rules Management to rapidly modify rules
- Collaboration portal for productivity across remote locations
- Support for any data format and system platform
- Business and technical views to speed deployment
- Comprehensive documentation and audit trail
- Comprehensive reporting and audit trail
For further information on improving your clinical trials productivity and drug or medical device development, contact 1-866-santeon (toll free) or info@santeon.com.
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