Euro-DMF/European Certificate of Suitability documentary guidance to Principals, including evaluation and submission.

Importation and distribution of API's (including Controlled API's) and pharmaceutical intermediates. Sourcing Formulation Dossiers in liaison with customer requirements for UK/E.U. Registration. Supply of finished formulations, including importation and distribution of bulk tablets (and finished packed tablets) via supply agreements linked to the corresponding Marketing Authorisation Holders. Contract Manufacturing - for select customers outsourcing products (tablets, capsules and liquids) where INTERPHARM can be influential in determining competitively priced products due to input of our Principal's API's.

Technology Exchange for Custom Synthesis - for the manufacture of API's or pharmaceutical intermediates to customer specification.