Регистрация лекарственных препаратов по правилам ЕАЭС

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Регистрация по процедуре взаимного признания

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Amendments

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Maximum Selling Price Registration

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Pharmaceutical Substances Registration

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Dossier Expert Review

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Quality Control Document Development

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SmPC and Package Leaflet Development

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Quality, Preclinical and Clinical Documentation Development

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eCTD Dossier Preparation

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Pharmaceutical Research & Development

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Preclinical & Clinical Studies

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package-leaflet-user-testing

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Independent Drug Quality Control

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Regulatory Affairs Department Services

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Pharmaceutical Substances Sourcing & Supply

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Project Management for Development, Technology Transfer, Localization & Contract Manufacturing

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