Contract Services

Kashiv Pharma provides clients with dosage form development for both conventional and challenging active pharmaceutical ingredients—from the preclinical phase to clinical manufacture. Multidisciplinary teams work closely with clients to clearly identify and understand their problems and needs. We focus on the physicochemical and biopharmaceutical properties of the compound and the dosage form requirements make decisions about drug-delivery platforms to develop the appropriate formulation—one that demonstrates the highest potential for performance, stability, and manufactureability.

For more information, please email contractservices@kashivpharma.com.

Choose a section to learn more about what Kashiv can do for you.

Preformulation

Our state-of-the-art preformulation laboratory is capable of conducting physicochemical characterization of new and existing drug molecules.
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Analytical R&D

With top-of-the-line cGMP facilities and instrumentation, as well as experienced scientists, Kashiv Pharma offers a full array of analytical services.
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Formulation Development

Kashiv offers formulation development and preclinical supplies for a full range of pharmaceutical oral dosage forms.
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cGMP Pilot Plant Manufacturing

Our FDA-registered site in Bridgewater, New Jersey, complies fully with State, OSHA, EPA, GLP and GMP Standards.
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  • Solutions for multiple challenges
  • Accomplished scientists
  • Proprietary technology platforms
  • Entire product life-cycle support