Benefit from our experience!
We help you with administrative issues
Because of our cooperation with many customers on the international level, our experts have acquired extensive experience in the field of Regulatory Affairs. Nowadays the conditions for the admission of amino acids and other pharmaceutical products differ from country to country, from region to region, and they are complex.
We gladly help you with the documents required for the registration of your pharmaceutical products, the correct interpretation of information in questionnaires and the provision of all necessary documents. AMINO possesses Drug Master Files and CEP certificates.
You can always be sure that AMINO fulfils the rules and requirements of the respective administration. We are subject to the supervision of the health and safety control office in Braunschweig, Germany and have the manufacturing permission according to the German Drug Act as well as a GMP Certificate. AMINO has also successfully undergone the strict control of the US American Food and Drug Administration.