A clinical trial is a crucial part of the drug research and approval process. The data obtained from clinical trials is critical for meeting regulatory compliance and ensuring a drug’s efficacy and safety for human usage.
Clinical trials have improved in accuracy and efficiency as technology has advanced, lowering the likelihood of drug failure. Clinical trial software and clinical trial management systems, such as EDC, eCOA/ePRO, and eConsent, have been combined with clinical trial automation software to collect data at each stage of the study in order to enhance clinical outcomes.

With increasing inclinations for incorporating technology into the drug development process, the clinical trial software market is expected to exceed USD 3,684 million by 2035, according to a recently published Roots Analysis research. As technology advances, the market is projected to see various creative developments that will transform the future of clinical trials.

These clinical trial software market trends will create various chances for the industry’s leading players.