Project overview
Our client sought a solution to enhance a platform that manages the entire clinical trial process, from initial planning to completion. We focused on addressing a key challenge of patient dropout and trial delays by developing new features for clinical study design and stakeholder communication. This included strategic trial planning based on patient availability across different regions and facilitating collaboration between clinical sites, sponsors and patients, including reporting and documentation.
Client background
A leading Contract Research Organization (CRO) that provides integrated clinical research services to pharmaceutical, biotech and medical device organizations worldwide. The company delivers fully integrated services across the entire clinical trial lifecycle – from study design and site activation to data analytics and regulatory support, with a focus on helping clients reduce time to market, cut costs and improve overall quality.
Goals
The primary objective of the project was to enhance a clinical trial management platform by introducing new features for greater efficiency. The focus was on improving clinical study design through strategic planning and facilitating and automating collaboration between key parties involved in clinical trials, such as CROs, clinical sites, sponsors, physicians and patients, with the ultimate goal of mitigating costly issues like patient dropout and non-responsiveness.
