As your drugs advance to the clinic, your organization will be faced with a broad spectrum of new requirements to plan, resource, document and track the latter staged of drug development and clinical trials. These critical steps bring with them a host of new software systems and organizational requirements. We have helped several companies navigate that transition and have domain and systems knowledge of systems that support:
- GxP studiesR
- Regulatory filings
- Clinical trial planning and operations:
- Electronic Data Capture (EDC)
- Clinical Data Management and Warehouses (CDM)
- Clinical Trial Management Software CTMS)
- Site management
- Site payments
- Targeted Source Document Verification (SDV)
- Clinical supply fulfillment)
- Clinical Data Analytics and Dashboards in TIBCO Spotfire
In addition, Boulder BioConsulting includes an expert that has designed and executed the critical late-stage clinical experiments that have elucidated a path to clinic for several drugs, particularly in the Immunology and Oncology spaces. This unique individual can help you with your late-stage development and clinical strategy, and guide you to a better path to the clinic.
