Monitoring medical research

Reviewing medical research

Description

Monitoring medical research involves systematically tracking and evaluating ongoing studies, clinical trials, and scientific developments to ensure ethical standards, data integrity, and public safety. This strategy aims to identify and address potential risks, misconduct, or inefficiencies, thereby safeguarding participants and improving research quality. Effective monitoring enables timely interventions, promotes transparency, and supports evidence-based decision-making, ultimately enhancing the reliability and societal benefit of medical advancements while preventing harm and misuse of resources.