Formulation Development

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Recipharm offer formulation development services for all dosage forms. We develop everything from simple formulations for early studies to more complex formulations suited for commercialisation.

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Finished Dosage FormsContract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)ParenteralsTabletsTransdermal PatchesStability TestingProject ManagementDrug Delivery Devices & SystemsParenteral ContainersLaboratory and Analytical ServicesFormulation developmentRegulatory AffairsContract Research Organisations (CROs)Testing, measurement, control, inspectionContract Packaging ServicesProductsServices

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Finished Dosage FormsContract Development and Manufacturing Organisations (CDMOs) and Contract Manufacturing Organisations (CMOs)Drug Delivery Devices & SystemsLaboratory and Analytical ServicesContract Research Organisations (CROs)Contract Packaging Services

Recipharm ABRecipharm is a leading contract development and manufacturing organisation (CDMO) headquartered in Stockholm, Sweden. We operate development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK and the US and are continuing to grow and expand our offering for our customers. Employing over 5,200 people, we are focused on supporting pharmaceutical companies with our full service offering, taking products from early development through to commercial production. For over 25 years, we have partnered with our clients throughout the entire product lifecycle, providing pharmaceutical expertise and managing complexity, time and time again. We conduct our business as we always have and continue to deliver value for money with each customer’s needs firmly at the heart of all that we do.

Formulation Development

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