Services
Galenica’s core competence is drug development for the pharmaceutical industry. We 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
We are CGMP compliant for production of clinical trial material of the most commonly existing dosage forms. Our analytical team utilizes a variety of analytical techniques in- cluding GC, HPLC, LS-MS-MS, NIR, DSC, laser diff raction, 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 cGMP production of clinical trial material. We welcome you to visit our site for audits or to discuss your project needs.
