At Chemo, we manufacture a broad variety of active pharmaceutical ingredients (APIs) and a full range of Finished Dosage Forms (FDFs) for both human and veterinary use in the main treatment areas.
We have a team dedicated to all pre- and post-production activities, from the transfer of manufacturing processes and analytical methods to regulatory support.
Portfolio of over 100 molecules and more than 50 pharmaceuticals, including steroids, antiulcer drugs, hormones, antifungals, prostaglandins, antihistamines, PPIs, respiratory drugs, antibiotics and oral hormonal contraceptives.
Diverse range of pharmaceutical forms with almost 200 different formulations, including tablets, capsules, granules, inhalers, injectables and suspensions.
We cover a broad range of different treatment areas:
Cardiology, gastroenterology, central nervous system, anti-infectives, respiratory, women's health, endocrinology, dermatology and urology.
We have an integrated quality and safety system in place for the product manufacturing process across all of our production centres.
We comply fully with regulatory requirements, including good manufacturing practices (GMP) and international guidelines and standards for the pharmaceutical industry, agreements included in product licenses, marketing authorisations, documentation submitted for registration with health authorities, requirements stipulated in internal documents created by the Corporate Quality Department and the Quality Guarantee observed at the group's plants.