Scope of Services

Peptido is registered with the U.S. Food and Drug Administration (FDA) and maintains its own US-DMFs, CEPs and additional regulatory approvals worldwide.

Peptido specializes in the synthesis of pharmaceutical active ingredients under cGMP conditions.

In addition to production, our strengths include the development of new synthesis routes for pharmaceutical active ingredients and their global regulatory submission.

The avoidance and minimisation of impurities, the identification of unknown related substances and degradation products, and stability testing of the developed active ingredients are integral parts of our work.

From research and development in the laboratory, to small-scale production in our pilot facility for regulatory purposes, and finally to routine synthesis at production scale – Peptido is a competent and flexible partner for its customers.

With extensive experience in working with national and international authorities, the global registration of our active ingredients is an established component of our activities.

Peptido performs organic syntheses at reactor volumes of up to 1.5 m³ and at temperatures ranging from -20°C to +120°C, including under inert gas atmosphere and cGMP conditions where required.

Please feel free to contact us.