Cooperate with Galenica

Tailor-made solutions for our partners.

Tailor-made solutions for our partners.

Galenica has a proven track record when it comes to pharmaceutical development, by having supported hundreds of clients in their pharmaceutical development programs through our company’s 20+ year history.

Our broad expertise in a wide array of dosage forms – oral, dermal, nasal and pulmonary – combined with on-site state-of-the-art equipment and a strong personal commitment has been the foundation of many successful collaboration. With an extensive range of analytical equipment available, as well as comprehensive stability study expertise, we work closely with our partners in every stage of the product development process.

At Galenica we can support our customers all the way from the earliest pre-formulation trials, through delivery of clinical trial material, of course also supporting with the necessary regulatory documentation. The flexibility in our multi-purpose GMP manufacturing facility ensures that even the most complex dosage form can be manufactured and supplied on time.

We work according to current GMP, ICH guidelines and pharmacopoeias and we are authorized and approved by Läkemedelsverket (Swedish Medical Products Agency) as well as EMA (European Medicines Agency).


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We understand what it means to bring something from a high conceptual level all the way to a commercial product.

Contact us at an early stage.

If you have any queries regarding a Galenica product or licensing opportunity, please send an email to: or fill in the form below.

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