What We Do

Koziatek Consulting is focused on providing outsourcing solutions throughout the entire pharmaceutical product and business lifecycle. We can connect your organization to our international network of CDMO/CMO/CRO/CRAMS companies that provide a wide range of contract services to include API development and manufacturing, pre-formulation studies, analytical method development, formulation development, clinical trial material manufacturing, clinical trial package services, scale-up, and low to high volume commercial manufacturing for almost all dosage forms. 

From start to finish, we can assist you from the earliest stages of development, to market launch, and commercial manufacturing. We provide guidance on finding high-quality manufacturing services for most finished dosage forms, including: small and large volume parenterals; solid dose; liquids; powders; and semi-solid formats. We can handle high potent API to include hormonal and cytotoxic API. If there is a unique technology not presently in our network, then we will find it for our clients. Our geographical capabilities span North America, Europe, and Asia.

Koziatek Consulting has a vast library of approved ANDA and European Market Authorizations and tech transfer dossiers. We can help you find, buy, sell, partner, or license generic and innovator drugs.

Our team can also find the hard to source comparator and Reference Listed Drugs (RLD) for you.

Have another need? Let us know!