Coding is an instrument which helps in bringing uniformity to the complete practice. Medical coding is compulsory mandate in many parts of the world, mainly USA and Canada. Medical coding is in itself a very professional aspect of medical practice. It helps in bringing harmonization to the practice and helps to remove the fault reporting in medical profession. Clinical trials are an important part of drug research which is often amalgamated with the medical practice. Regions other than America are becoming hot spots with respect to clinical research and clinical trial perspective. Though certain areas under clinical trials and clinical research, coding is compulsory but it is somehow restricted to clinical data management especially in the region of “Data Review and Discrepancy Management”. The present letter especially focuses on bringing coding to complete clinical research and clinical trial perspective, hence bringing in clearer harmonization in clinical trials and clinical research thus restricting the fraud claims by the investigators and sponsors to bring false products in the market through false FDA approvals.
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