Clinical Data Management in Clinical Trials: Clinical trial data usually flows from the patient to a clinical study report or publication. The data goes through several steps between the collection, verification, and analysis. Most clinical research stakeholders look at studies using this workflow and discuss...
Read More
Clinical data management (CDM) is the process of collecting and managing research data following regulatory standards to obtain complete and error-free quality information. Keeping federal, state, and local regulations in mind, the goal is to collect as much data as possible for analysis. Clinical data management...
Read More
Clinical Data Management in clinical research is an important stage that generates high-quality, reliable, and statistically sound data from clinical trials. It reduces the time it takes from drug development to marketing. Throughout a trial, the quality of various CDM procedures, such as Case Report...
Read More
Data is at the heart of any clinical study and guides drug development decisions. A new therapy's ability to receive approval from regulators such as the Food and Drug Administration, as well as other stakeholders, including payers and health technology assessment (HTA) organisations, is dependent...
Read More
From a financial standpoint, drug developers want to make sure the data they provide to regulatory agencies is accurate; from an ethical standpoint, clinical data drive treatment decisions and, ultimately, patient health. Clinical data quality and integrity are critical for both of these reasons. Although data...
Read More
Experimental research has garnered widespread prominence in today's medical industry. With new technologies cropping up each year, the field of medicine has experienced various advances that have opened the gates to the possibility of promoting better healthcare. This calls for better and more efficient clinical...
Read More