LIST
|
№ |
Names |
Country |
1 |
Food and Drug Administration (FDA) |
USA |
2 |
Notified European bodies to issue the European Certificate of Conformity (CE) |
European Union |
3 |
European Medicines Agency (EMA) |
European Union |
4 |
Pharmaceuticals and Medical Devices Agency (PMDA) |
Japan |
5 |
Ministry of Food and Drug Safety (MFDS) |
Republic of Korea |
6 |
Medicines and Healthcare Products Regulatory Agency (MHRA) |
Great Britain |
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See also:
|
Pharmacopoeia CommitteeTasks of the Pharmacopoeia Committee:- examination of normative documents for medicines subject to registration and extension of the term of registration; - systematic revision of normative documents for medicines with a view to improving their quality and improving the methods of control; - examination and preparation for approval of additions and amendments of the... Read more |
Department of RegistrationTasks of the Registration Department:- after the adoption of the application for registration, conducts the initial (preliminary) examination of the application and attached registration documents and samples of medicines, medical devices and medical equipment; - conducts appropriate correspondence with the applicant on the... Read more |
Pharmacological CommitteeTasks of the Pharmacological Committee:- conducts examination of administrative, pharmacological, toxicological and clinical parts of registration documents of pharmacological and (or) medicinal products; - conducts examines and re-examines documents of pharmacological and (or) medicinal products with the involvement of independent experts; - decides on the use of the medicines without clinical trials in the... Read more |