Before the drug will enter the market in Kazakhstan and appear in a pharmacy, state registration of medicines will be required.
This is a set of measures aimed at checking the quality of the drug, its effectiveness and safety. Also, during registration, the results of clinical and preclinical trials, the compliance of the product with international
standards are assessed. The main goal of the procedure is to provide the population with quality medicines (hereinafter - drugs) with proven efficacy.
Registration of medicinal products is a core business of the GO PHARM group of companies, which is one of the leaders in the field of registration among international consulting companies. We guarantee
strict control at every stage of the procedure, we comply with the established deadlines.
Benefits of cooperation with professionals
Self-registration of medicines is a complex and lengthy process that requires deep knowledge of the regulatory framework, the specifics of communication with the regulatory body. Without them, you risk spending
a lot of time and incur significant financial losses.
Experienced specialists of "GO PHARM" will take care of all the issues related to the state registration of Medicinal Products. Our team consists of 73 specialists in various areas of regulatory activity. We
develop personalized solutions for clients and respect confidentiality.
What drugs can be registered?
- Active pharmaceutical ingredients.
- Biotechnological medicines.
- Medicinal herbal raw materials.
- Immunological drugs.
- Original drugs.
- Homeopathic medicines.
- Generics (drugs with an active substance that is identical to the substance patented by the original developer MD)
- Biosimilar medicines (biosimilars)
- Medicinal products of biological origin.
- Bulk products MD (metered-dose medicines that have passed all stages of manufacture, with the exception of packaging).