c-LEcta GmbH services

Our economic success is based on our ability and willingness to innovate, the high quality of our products for regulated applications, and our endeavors to continuously advance and improve.

To ensure reliable supply of our products that fully meet the requirements of the target markets, we create and maintain highest quality authorization dossier. We have gained extensive experience in the authorization of food enzymes and additives in the European Union, the USA, and other regions. By submitting Type-II Drug Master Files for our products, we support our customers in the pharmaceutical sector by reducing their regulatory challenges during development and authorization processes. We also have solid expertise regarding compliance with REACh and TSCA requirements.