Just tell us the specifics of what you need. We've been providing contract manufacturing services for more than 40 years. We can take your proprietary compound from concept to commercial production, from grams to multi-metric ton quantities.

Ferro Phanstiehl can provide custom sythesis of new chemical entities (NCEs), specialty carbohydrates and injectable quality, cGMP pharmaceutical ingredients, in commercial quantities.

We'll deliver your product at the level of purity you choose. Just ask us. You need a pharmaceutical grade product manufactured to cGMP standards? Need a low endotoxin product for use in an injectable drug formulation? Need special analytical testing?

Our capabilities include process scale-up, development and process validation according to cGMP guidelines. Our facilities and equipment are configured to produce high-purity, low-endotoxin compounds, including potent (highly active toxic or cytotoxic) drugs under cGMP conditions.

As a long-time manufacturer of low-endotoxin carbohydrates, injectable grade excipients, active pharmaceutical ingredients (API's) and pharmaceutical intermediates, Ferro Pfanstiehl can establish and maintain U.S. and European Drug Master Files (DMF's) and European "Certificates of Suitability" for your product. Ferro Pfanstiehl is here to help you get your compound to market—seamlessly bridging the critical gap between product development and regulatory approval.

Need more information?  Contact us or call 1-800-383-0126