About Us
About Us
Keyfiyyət siyasəti
Import of Medicines
Documents
Documents required for the import of medicines
Documents required for the import of medical supplies
Letter samples
Registration of Medicines
Department of Registration
Legislation
Expertise of FS
About the approval of the “Guideline for the Expertise of Food Supplements”
Bioloji fəallığa malik qida əlavələrinin ekspertizadan keçirilməsi QAYDASI
1. Ümumi müddəalar
2. Əsas anlayışlar
3. Bioloji fəallığa malik qida əlavələrinin ekspertizasının həyata keçirilməsi qaydası
4. Bioloji fəallığa malik qida əlavələrinin tərkibinə dair tələblər
5. Bioloji fəallığa malik qida əlavələrinin qablaşdırılmasına dair tələblər
6. Bioloji fəallığa malik qida əlavələrinin istifadə təlimatının tərtibatına dair tələblər
Bioloji Fəallığa Malik Qida Əlavəsinə dair - EKSPERTİZA RƏYİ
Result of the Expertise of FS
Result of the expertise of FS 2018
Result of the expertise of FS 2019
Result of the expertise of FS 2019
Result of the expertise of 2022
Control on Medicines
Control on Medicines
Legislation
Laboratory
About the Quality Control Laboratory
Pharmacovigilance
General information
Legislation
Information for healthcare professionals
Information for Patients
Pharmacovigilance dictionary
Reporting forms
Onlayn bildirişlər
Contacts
Private medical institutions
Legislation
Rates
Contacts
En
Az
Ru
Registration of Medicines
Legislation
Rules:
On approval of the "Rules for state registration and maintenance of the register of medicines"
RULES for state registration and maintenance of the register of medicines
List of documents required for registration of changes in medicinal product
Rules for the expertise of medicinal product
About approval of "Rules of expertise of biologically active food additives"
RULES for examination of biologically active food supplements
Annexes:
Annex 1. Application for state registration of a medicinal product
Letter of application for state registration of the medicinal product
Letter of application for re-registration of the medicinal product
Letter of application for state registration of changes in the registration documents of the medicinal product
Annex 2. Application for state registration of API (Active pharmaceutical ingredient) in the Republic of Azerbaijan
Annex 3. Documents for registration of medicinal product produced in a foreign country
Annex 4. Documents for registration of API (Active pharmaceutical ingredient)
Annex 5. Documents for registration of domestically produced API (Active pharmaceutical ingredient)
Annex 6. Documents for re-registration of medicinal product produced in a foreign country
Annex 7. Documents for Re-registration of domestically produced API (Active pharmaceutical ingredient)
Annex 8. List of requirements for medicinal product labeling
Annex 9. List of requirements for instructions for use of the medicinal product
Annex 10. List of requirements for instructions on the use of medicinal product (for consumers)
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