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MAA dossier – review and compilation of modules 1 to 5
MAA dossier – review and compilation of modules 1 to 5
MAA dossier – review and compilation of modules 1 to 5
As the European regulatory system strives to ensure delivering safe, efficient, and quality medicines to their citizens the documents submitted to the health agencies should comply with all the ICH requirements as well as country specific requirements related to submission for marketing authorization. We provide end to end services for dossier compilation with utmost accuracy and in compliance with all the regulatory requirements.