Our GMP facility in Frellstedt, Germany, is state-of-the-art, fulfilling all requirements associated with GMP production, such as validated production equipment, sterile zones for handling open products, and a highly complex arrangement of airlocks.

Continuous upgrades in our GMP facility and new investments in technologies and production capacity provides customers the assurance they require in obtaining reliable supplies of amino acids, now and in the future.

All products are registered with international health authorities, such as the United States Food and Drug Administration, under a Drug Master File number. All AMINO products meet the high quality requirements of the Pharmacopoeias, such as EP/DAB, USP and Food Chemical Codex. We are glad to offer regulatory support for our customers.