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July 07, 2015 5:40 AM ET


Company Overview of DSM Pharmaceuticals, Inc.

Company Overview

DSM Pharmaceuticals, Inc. provides custom manufacturing services to the pharmaceutical and biopharmaceutical industries. It offers a range of manufacturing services in the areas of steriles, and orals and topicals, including dose form manufacturing, scheduled drugs, clinical manufacturing, fill finish manufacturing, aseptic filling, terminal sterilization, cold storage, ampoules, vials, and lyophilization. The company was formerly known as Catalytica Pharmaceuticals, Inc. and changed its name to DSM Pharmaceuticals, Inc. in December 2001. The company was founded in 1993 and is based in Greenville, North Carolina. DSM Pharmaceuticals, Inc. operates as a subsidiary of DSM Pharmaceutical Produc...

5900 Martin Luther King Jr. Highway

Greenville, NC 27834-8628

United States

Founded in 1993





Key Executives for DSM Pharmaceuticals, Inc.

Chairman of Managing Board
Age: 67
Deputy Chairman of Managing Board
Age: 66
Member of Managing Board
Age: 56
Member of Managing Board
Age: 56
Compensation as of Fiscal Year 2015.

DSM Pharmaceuticals, Inc. Key Developments

Discovery Laboratories Inc. Enters Master Services Agreement with DSM Pharmaceuticals, Inc

On October 24, 2013, Discovery Laboratories entered into a Master Services Agreement with DSM Pharmaceuticals, Inc. DSM is a contract manufacturing organization (CMO) with experience in the manufacture of lyophilized products and with whom the Company has completed a technology transfer of its lyophilized KL4 surfactant manufacturing process. The Agreement is intended to support further development and manufacture of the Company’s lyophilized KL4 surfactant for the Company’s pipeline programs, primarily AEROSURF. Pursuant to the Agreement, DSM will perform certain development and manufacturing activities relating to the Product as may be requested by the company and as may be agreed by the parties in one or more statements of work. Such activities could include but are not limited to equipment procurement and installation, validation master planning, regulatory support, quality assurance support, manufacture of engineering lots and development lots to support the Company’s preclinical, clinical, research and development activities, potential scale-up activities and potential manufacture of process validation lots.

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