The seminar will study in detail:
- Rights and obligations of businesses involved into the circulation of medicines;
- Licensing of pharmaceutical practice;
- Accreditation of businesses involved in the circulation of medicines;
- State registration of medicines, their certification, labeling, advertising, wholesale and retail trade;
- Fundamental principles and requirements of GDP/GPP/GMP (Good Distribution Practice, Good Pharmacy Practice and Good Manufacturing Practice)
The Seminar will also cover:
a) Concept of quality assurance for pharmaceuticals (Good Distribution Practice, Good Pharmacy Practice and Good Manufacturing Practice);
b) Principles and provisions of GxP quality guidelines and regulations;
c) A contemporary approach to the introduction and application of GxP quality guidelines (local and foreign experience)
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