Medical & Regulatory Services - Inhaled Products

Product description

Our formulation, device and development services are supported by our medical, regulatory, device vigilance and pharmacovigilance teams to safeguard your programme and ensure the smoothest path to product approval.

Our in-house team can support with:

Global regulatory development strategy and submission expertise (NCEs and generics)
Medical devices and combination products including compliance with the EU Medical Device Regulation (MDR)
Global pharmacovigilance and device vigilance capabilities
Clinical strategy and protocol development
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