Department of Clinical research, Geethanjali College of Pharmacy, Cheeryal, Keesara, Hyderabad, India
Mini Review
Administration of Data Management in Clinical Research: Mini Review
Author(s): Divya Dara*
A crucial stage in clinical research is clinical data management (CDM), which produces high-quality, trustworthy, and statistically sound data from clinical trials. This results in a significantly shorter period of time between drug development and release. From the beginning to the end of a clinical trial, CDM team members are actively involved. They must have sufficient process knowledge to support upholding the CDM processes high levels of quality. At regular intervals throughout a trial, various CDM processes-including Case Report Form (CRF) designing, CRF annotation, database designing, data entry, data validation, inconsistency management, medical coding, data extraction, and database locking are evaluated for quality. To meet regulatory requirements and stay ahead of the market through quicker product commercialization, there is a greater need to strengthen CDM standards in the.. View More»
Spanish 
Chinese 
Russian 
German 
French 
Japanese 
Portuguese 
Hindi 
