Drug Development
Because of the immense value real world evidence harnesses, life sciences and healthcare organizations are investing a lot of time and means to make the several different clinical data sources interoperable and unlock its value for drug development, approval and optimization.
Unfortunately, many different standards are used in life sciences and healthcare. A one-size-fits-all concept for this digitalization does not exist just yet. And without a common ground, you cannot integrate data and you won’t unlock the real value of your data.
Thanks to our cross-functional industry focus, we can help to integrate clinical data and accelerate drug development in your life sciences organization.
Analyze
We kick off with a clinical data maturity check providing an in-depth view of your current clinical data management process. We identify which data can be useful and how it can be accessed to gain insights to fuel decisions and add value to your process.
Integrate
We harmonize your clinical data sources (SNOMED, CDISC, ICD10, DICOM, MedDRA, WHODrug, LOINC, OMOP OHDSI) to keep only one platform for automated Data Collection (ePRO, ePerfO, eClinRO, eObsRO), Data Review, Data Analysis and Submission packages.
Change
We implement change management processes across the organization to make sure we grasp every benefit.
Compliance
We create end-to-end visibility of your development chain when you control your entire data flow. For this, we will apply data integrity by design principles in your organization.
Faster
You will have integrated and clearly visualized this data integration reduces the lead-time and costs of clinical data management
Error-free
You won’t have to insert information that’s still on paper, increasing the quality of your data
Accuracy
Combining more data adds intelligence and accuracy to the development process