We can support you across all regulatory activities. Our range of services covers development projects, full generic or bibliographical applications for marketing authorisation, traditional registration, national and international procedures, including variations and renewals, dossier updates and the extension of pharmaceutical product lines.
We are also expert partners in the certification of pharmaceutical-like medical devices and drug-device combination products, in-licensing and out-licensing, the purchase and sale of products and all types of due diligence pertaining to dossiers and documents in this context.
We aim to reduce your workload - whenever it comes to regulatory work, development projects and marketing authorisation projects. With our knowledge and expertise, we can manage your projects successfully, even within tight deadlines.
'Individuality, intelligence, ingenuity': this is our promise. It means a collaboration that is smart, tailored to your needs and based on close partnership.
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