Registration of drug is a process of authorizing the input to the market and its inclusion to the list of authorized products. It is carried out at international or national level, which falls under the competence of the relevant drug agencies. This process involves several activities, from income and assessment of applications, through the verification of the quality, safety and efficacy to the entry in the list of authorized products. However, by registration of the drug, the evaluation process does not end. Drug is undergoing by various changes, after 5 years is issued to renewal, it may develop drug transfer to another holder or its revocation.
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