WHy Collect Data In A Registry?

Registries have long been an effective tool for gathering data. The data provided through registries generates important insights into patient characteristics and behaviors, standards of care, treatment landscape(s), and long-term clinical outcomes of a pharmaceutical or medical device product.

Recent advances in collecting and leveraging real world data (RWD) to generate real world evidence (RWE) have exponentially increased the value of registries by allowing companies to understand and differentiate their products and development portfolios & tactics.

RWE is evidence on health care that is generated from data derived from multiple sources outside of the typical clinical research setting. It helps provide information that is relevant and meaningful to stakeholders, that often could not be collected from the traditional randomized clinical trial model.

Sponsors should keep certain factors in mind when trying to maximize the reliability of the data collected in the registry. These factors include:

  • Data accrual – are the methods of colleting the data sound and suitable?

  • Data integrity – do registry processes and personnel minimize errors and eliminate the possibility of bias?

  • Data security and confidentiality – are there privacy controls in place to protect the data?

How Can WEP Clinial Help?

At WEP Clinical, our clinical and commercial teams work together to share best practices, interpretations, and knowledge to ensure the success of your registry. We are committed to working with you to deliver registries that will generate the RWE needed to gain insights and add value to your R&D, early access and/or commercialization efforts.

WEP has the capabilities to assist with your patient registries needs whether they are:

  • Disease-specific

  • Drug/treatment-specific

  • Prospective or Retrospective

Our team will work with you to understand the purpose and goals of your registry and advise on the types of data to collect. Examples of data to collect include:

  • Demographic and clinical information

  • Treatment information for the disease of interest

  • Health-related outcome information

  • Quality of life information

  • Pregnancy-related information

  • Patient satisfaction surveys

We will then design, develop and manage your registry to meet your goals for generating RWE.

WEP Clinical will ensure that the evidence you generate is meaningful and can be used to support decisions being made by and for key stakeholders, including patients and physicians, regulatory bodies, health plan providers and reimbursement agencies.

If you would like more information on our registry services & capabilities, please contact us using the link below: