Research Design

We utilize rich and comprehensive analyses of relevant data to provide specific and actionable answers to your questions. We’ll work with you to evaluate your product's performance in the context of real-world patient experiences.

IRB Submission & Management

Regulatory submissions can be burdensome and time-consuming. We offer expertise and efficient processes for securing approval in required pre-study reviews (IRB and FDA if required).

Primary & Secondary Data Collection

We’ll create a roadmap for study completion, to be created and executed through an agile approach. We can help fine-tune research questions and provide robust studies of these research questions using distinct and relevant data from validated tools.

Data Analysis

Insights gained through advanced statistical analyses, as well as high-quality and rigorous qualitative explorations of patient experiences, will provide findings with high integrity and fidelity in relation to your research questions.

Dissemination (Including Publication)

We offer expertise in translating study results to peer-reviewed scholarly and professional forums. This ensures that your therapeutic's story will be accessible and part of the public knowledge base relevant to your therapeutic.