The pharmaceutical manufacturing activities carried on the site of Algorithm cover the manufacturing and packaging of non-sterile oral and topical dosage forms: liquids, tablets, capsules, suppositories, granules for suspensions, creams and ointments.
Algorithm maintains a comprehensive Quality Management System that ensures consistency in product quality, incorporates GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices) and complies with regulatory, licensors and ISO 9001:2000 requirements.
A continuous monitoring system is in place for adequate and strict application of validation requirements ensuring a “quality at the source” through the different steps of production and distribution.
The source of raw materials is exclusively through the licensors or their approved suppliers, for products under-license, and through FDA or EMEA approved suppliers for generics.
The manufacturing facility is periodically audited by licensors and by the health authorities of all the countries where the products are marketed.