We fully comply with 62/2011/UE Directive requirements as well as national pharmaceutical law. We are registered in national Registry as well as in EudraGMDP as an API importer and distributor.
On Customer’s request, we globally search for substances perfectly matching the requirements of a certain project. We actively support not only in substance search for new projects on R&D basis but we also seek for alternative suppliers to fully commercialised products.
We are thoroughly analysing the supplier’s market on a constant basis including the quality of offered raw materials, availability, manufacturing conditions, implemented quality systems and price level.
We are tracking warehousing and transport conditions (temperature, humidity) of all imported and distributed APIs and all other substances if required. We control the conditions from manufacturer’s warehouse up to delivery to the final customer. We organise transport at 15°C - 25°C, as well as freeze, refrigerated or custom conditions.
In collaboration with the manufacturer, we deliver to the Customer complete product data, which simplifies and speeds up the R&D process. We support in the selection of compatible ingredients and solving particular technological problems.
We deliver full registration documents and support our Customer’s in the registration process. We also offer a wide range of ready registration dossiers for prompt market commercialisation.
In collaboration with a manufacturer and final Customer, we organise laboratory and trial production tests. Such cooperation often supports in a prompt and successful conclusion of the R&D stage and launch of a ready product.
On Customer’s request or together with the Customers we organise supplier’s assessment audits.
Continuous improvement, research and extension of our supplier’s database from all around the world - all these make us an outstanding partner.