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- Reduce capital costs compared with multiple, expensive applications (that have low to no integration capabilities), as CRIS is installed completely integrated, enabling you to capture, archive and report on data across your entire clinical enterprise.
- Eliminate unnecessary acquisition and implementation costs, and reduce demands on your management team, legal counsel and IT department compared with contracting multiple software suppliers. Choosing CRIS means choosing a total solution delivered through a single vendor, ultimately reducing company downtime during the decision-making and implementation process.
- Gain more control over the clinical trial process, as data integrated by CRIS helps you:
- Determine any necessary mid-study course corrections vs. discovering protocol deficiencies during the FDA review process.
- Quickly access timely, fact-based data for management, the public, the FDA, investors, investigators, internal staff and corporate partners.
- Make real-time decisions and create efficiencies in day-to-day business through secure information transparency held in a central repository accessible across the enterprise.
- Hedge risk against failure to comply with the growing volume of increasingly stringent FDA standards (including the Code of Federal Regulations, Section 21, Part 11), as Sierra delivers CRIS fully compliant and offers periodic CRIS updates reflecting the latest FDA requirements.
- Streamline your installation process to an unparalleled minimum with CRIS' easy installation and maintenance procedures, including full data migration and validation support.
- Minimize interruptions during deployment, as CRIS is "database-agnostic," allowing a migration path from any database and seamless data integration with any existing solution or everyday application.
- Purchase once, implement quickly, as CRIS is one-click configurable to the unique protocol demands for drugs, devices, biologics, IVDs and combination products.
- Maximize your expertise through Sierra MRC, scientists and medical experts guiding start-ups and first time clinical trial sponsors, and supporting large corporations with stretched resources, in the planning, development, execution and analysis of their clinical trials.
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