Medical & Regulatory Services - Inhaled Products

Medical & Regulatory Services - Inhaled Products

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Medical & Regulatory Services - Inhaled Products
Medical & Regulatory Services - Inhaled Products

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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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Contract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)Drug Delivery Devices & SystemsRegulatory AffairsPharmaceutical Machinery & TechnologyMedical DevicesProductsServices
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Contract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)Drug Delivery Devices & SystemsPharmaceutical Machinery & Technology
Vectura Ltd.Vectura integrates formulation, device and development capabilities to offer a broad range of services to help customers bring inhaled medicines to market. Vectura offers comprehensive services from the pre-clinical stage of development (including preclinical toxicology testing), when customers are looking to overcome complex inhaled formulation challenges, select a delivery device and move quickly to the clinic. With expertise in powder and liquid formulations, as well as a portfolio of proprietary device and ...

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