There are certain critical requirements needed in order to define a drug. The fundamental requirement is that the drug should have an identification number. The drug identification number is composed of eight digit numbers that are uniquely designed for each of the drugs which is commonly used in Canada.
The drugs are only allowed in the market once they pass the Therapeutic Products Directorate requirements. Moreover the process ensures that the drug complies with the legal requirements and that they do not pose any threats to the users. In addition, the process ensures that certain information about the drugs is easily identifiable including their prescriptions and the quality that is being offered.
The drugs are only allowed in the market once they pass the Therapeutic Products Directorate requirements. Moreover the process ensures that the drug complies with the legal requirements and that they do not pose any threats to the users. In addition, the process ensures that certain information about the drugs is easily identifiable including their prescriptions and the quality that is being offered.
Techniques of identifying | Drug Identification
There are several techniques that are usually used when it comes to the identification process. The common means is the use of codes that include:
· Procedural codes
· Diagnostic codes
· Outcomes codes
· Pharmaceutical codes
· Topographical codes
The above codes ensure that the drugs are appropriately classified to suit their functions. In addition the codes ensure that the correct drugs are placed in the appropriate categories.
The criteria used in Drug identification
There is a simple process that is usually used in the drug identification process. First, the drug is to be manufactured, after which the drug is to be tested appropriately in order to gauge whether it qualifies to be a drug. This is done specially by the medical experts. The status of the drug is then ascertained and if successfully, the drug is allocated a unique code that consists of digits. The drug is then allowed in the market and its prescription is also designed for both on shelf and pharmaceutical requirements. The drug is regularly monitored while in the market to ensure that it still meets its prior requirements and safe for its intended use.