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Inspections History

Hovione sites are periodically inspected by the local and external authorities. All sites are FDA approved and with exception of New Jersey site all have EU GMP certificates.

Regulatory support

Hovione has filings with every world health authority that has a DMF system for APIs such as FDA EDQM, PMDA, MHRA, HPRA, Infarmed

Inhalation grade particles

Hovione is a global expert in particle engineering, an essential technology when developing inhalation drug products.

Dry Powder Inhalation formulation development

Hovione has considerable inhalation experience that allows us to implement strategies including conventional carrier based, neat (drug-alone) or composite particle formulations.

Customers

Full transparency for your project anywhere at any time.

Inhalation devices

Hovione’s inhalers offer our business partners access to simple, multipurpose, easy to use, globally competitive alternatives for inhalation delivery devices.