You are working for a small-to-midsized biopharma (SMB) or a biosimilars generics pharma company with a few clinical trials. Your company is outsourcing most activities to CROs, and your small biometrics team manages many deliveries from multiple different CROs simultaneously.
Your challenge
SMB biopharma and biosimilars generics pharma companies often fully outsource the management of clinical trials to CROs, typically working with a diverse range of partners. This creates a need for strong oversight and effective collaboration management. To prepare for regulatory submissions, sponsors must ensure all study deliverables from CROs are handled within a validated environment and apply their own quality control methods to verify these deliverables.
Our solution
entimICE FastTrack offers flexible hierarchies to accommodate a wide range of requirements and use cases. It provides two streamlined options for data exchange between sponsors and multiple CROs.
In the first option, CROs upload and retrieve data via a secure dedicated staging area, from which data can be automatically brought into entimICE FastTrack and trigger initial workflows.
In the second option, CROs work directly within the platform, delivering data exactly where the sponsor needs it for further processing.
A clear separation of permissions ensures that each CRO has access only to their specific data delivery points, thus maintaining security while enabling efficient collaboration.
Additionally, entimICE FastTrack supports customizable workflows, allowing sponsors to define the appropriate level of quality control based on the type and source of data received from each CRO.
Take a closer look at the features and performance benefits we’ve developed to bring more speed and precision to every stage of your clinical trial services.
