A study on investigating operational management tools and methodologies to improve the efficiency in patient-centric clinical trials in bio-pharmaceuticals.

Abstract

This approach, in modern healthcare research, is known to emphasize  placing the patients at the center of the trial process. Operational management tools and strategies would thus be necessary in this process together for sustainable development of patient centric otherwise create inefficiency in the trial process and noncompliance. Against this backdrop, this study would assist in exploring the possibility of integrating operational management models within the patient-centric clinical trial, that is how strategies associated with enhancing data collection and management, informed consent, and lifestyle of patients may be embraced. It explores the need for adopting customized management of operations to optimize trial procedures, yet with awareness about patient's needs and rights. Topics include advanced technologies used in data collection and management, proper and informed consent procedure, and overcoming legal barriers.For the most part, this paper entails a comprehensive review of factors that are widely relevant in determining better efficiency and effectiveness of patient-centric clinical trials. Ultimately, these insights lead to sustainable practices in healthcare research, and in influencing  sustainable societies for patient outcomes while providing practical implications for practitioners on how best to implement these methodologies in their patient centric  trial processes.