Compilation of EU eCTD Dossier and management through the product life-cycle

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We offer services of Regulatory Affairs and Market Access to pharmaceutical companies, aimed to the development and marketing authorization of drug products as well as to the dossier maintenance during its Life Cycle.
Studio Governatori proposes consulting services in the following areas:
► Drug Product Development and CTD Dossier Preparation
► Post approval Dossier Maintenance
► Scientific Documentation
Delivery in 30 day(s)
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