Study CRF is a process which involves studying case report forms from clinical trials as well as ensuring that data is logged accurately. Clinical trials are often run to very strict standards of data compliance. This is because the results of clinical trials could influence how a drug or medicine is produced and could pose a risk if built up incorrectly or with poor or inaccurate data.
How Can Data Accuracy Be Improved?
In order to ensure that accurate data is used by clinical trials companies , there are a number of different policies and procedures in place. One of these policies is CDISC standards. Practically any clinical trial which is being undertaken needs to be subject to these standards. …