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After the experimental stage of development associated with the search for a biologically active compound, the creation of an adequate stable dosage form, the selection of optimal dosing regimens, an experimental development of the drug and its biopharmaceutical tests are carried out. They work out production regulations and create a Pharmacopoeia article, the drug is carefully checked, standardized and controlled by the Pharmacopoeial Committee of the Ministry of Health and Social Development of the Russian Federation. Conduct extensive pharmacological research and clinical trials organized by the Pharmacological Committee of the Ministry of Health and Social Development of the Russian Federation, as a result of which they decide on the possibility of using it in medical practice.

And only after receiving positive conclusions from the committees, it is officially registered with the Ministry of Health of the Russian Federation.

By the time a new drug is introduced to the pharmaceutical market, it is necessary to carefully familiarize yourself with the standardized official information about it and, based on the amount of pharmacological knowledge, skillfully use new data in your professional activities to conduct advisory work on comparative analysis with a rational choice of drugs.

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