GMP Production

XSpray offers particulate manufacturing meeting US and EU regulatory standards. Your API/DS is processed under GMP conditions, providing high quality drug particles and powders for use in clinical studies.

Manufacturing is carried out in collaboration with Galenica AB, an established Swedish CRO based in Malmö, Sweden. Galenica operates state-of-the-art GMP suites and is authorized and audited by the Swedish Medical Agency for GMP production of clinical trial material for Phase I-III. In addition to manufacturing, packaging and release testing services are also available.