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• 2016 - actually Organization of the audits, professional support, consulting, interpreting and translation for Regulatory GMP inspections according to according to the GMP standards: Eudralex, PIC/S, WHO, Order 916 (Russian GMP), Resolution No. 77 (Rules of the Eurasian Economic Union) carried out in the pharmaceutical (human and veterinary) and API sites. More than 50 regulatory inspections assisted in Europe and South America • 2016 - actually Translation of pharmaceutical documents: Registration Dossier, Marketing Authorisation Application, DMF (open and closes parts), drug safety profile, regulatory documentation, leaflets, CAPA documents, inspection reports, Site Master File, chemical synthesis flowcharts, etc. • 2019 – interpreter during Farmaforum Madrid 2019. Translation of Pharmaceutical, Biopharmaceutical and Laboratory documents for Russian companies involved in the Pharmaceutical business. • 2018 – interpreter during CPhI Worldwide Madrid. Main topics: APIs, pharmaceuticals, custom manufacturing, excipients, fine chemicals and intermediates products.
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