Galenica AB
Medeon Science Park
Visiting address:
Per Albin Hansson väg 41,
Malmö, Sweden
Phone +46 (0)40 32 10 95

Galenica’s core competence is drug development for the pharmaceutical industry. Galenica are experts at pharmaceutical and analytical development/validation, and production of Clinical Trial Material (CTM) for Phase I – III.

Supporting pharmaceutical product development and CTM production for:

  • Solids:
    • Tablets
    • Pellets
    • Hard capsules
    • Powders
  • Semi-solids:
    • Creams
    • Ointments
    • Gels
    • Suspensions
    • Emulsions
    • Suppositories
  • Liquids
  • Other non-traditional dosage forms:
    • Medicated chewing gums
    • Medicated shampoos

Galenica are GMP compliant for production of clinical trial material of the most commonly existing dosage forms. The analytical team utilizes a variety of analytical techniques including UPLC, HPLC, DSC, laser diffraction, for specialized method development, release testing of produced CTM and monitoring of stability studies.

Galenica is authorised and audited by the Swedish Medical Product Agency for the GMP production of clinical trial material. Welcome to visit our site for audits or to discuss your project needs.