Registration/renewal/variation/withdrawal processes of the medicinal products in Republic of Kazakhstan, Kyrgyzstan and Armenia Batch certification of medicinal products Identification the regulatory issues (current/ potential) in the area of responsibility and search for the best solutions to solve/to avoid problems and negative impact on the business. Close interaction and participation in the meetings with colleagues from BD department regarding new products development and BUs regarding EPs. Maintenance of regulatory process and prompt reaction on any regulatory changes and new requirements. Interaction with HLMs/country strategist/GCMC group to idettify any gaps and other issues, that can influence preparation of the documents or the products intended for registration and already marketed in particular country.

Registration/renewal/variation processes of medicinal products, medical devices Registration of dietary supplements Declaration/certification processes Import license for samples and finished products Preparation of layouts and instructions for medical use PV activities