Contract development and manufacturing organization

Contract development and manufacturing organization

A Contract Development and Manufacturing Organization (CDMO) is an organization that serves the pharmaceutical industry and provides clients with comprehensive services from drug development through manufacture.

Services offered by CDMOs include, but are not limited to: pre-formulation, formulation development, stability studies, method development, pre-clinical and Phase I clinical trial materials, late-stage clinical trial materials, formal stability, scale-up, registration batches and commercial production.

Evolution of CDMOs

The pharmaceutical market uses outsourcing services from providers in the form of contract research organizations (CROs) and contract manufacturing organizations (CMOs). In recent years, the concept of a comprehensive single-source provider from drug development through commercial manufacture has emerged. This concept has been implemented by providers known today as contract development and manufacturing organizations (CDMOs).

CDMOs are a response to the competitive international nature of the pharmaceutical market as well as the increasing demand for outsourced services. [Taylor, Phil. “Outsourcing of production gaining pace in big pharma” ( [http://outsourcing-pharma.com/news/ng.asp?n=85511-ms] ), Outsourcing Pharma.com, May 27, 2008. Retrieved 7-3-08.] The best-positioned service providers focus on a specific technology or dosage form and promote end-to-end continuity and efficiency for their outsourcing clients. With lower-cost international manufacturers capturing an increasing percentage of the contract manufacturing market, specialization may be an effective hedge against loss of market share. [Spurgeon, Tom. “Continuity and Connectivity: We Can Do That, Too” “(subtitle) Are CDMOs the Next Big Thing?” ( [http://contractpharma.com/articles/2008/03/continuity-and-connectivity-we-can-do-that-too] ), Contract Pharma, March 2008:70–74. Retrieved 7-3-08.]

Advantages of CDMOs

Outsourcing to a CDMO allows the pharmaceutical client to expand its technical resources without increased overhead. The client can then manage its internal resources and costs by focusing on core competencies and high-value projects while reducing or not adding infrastructure or technical staff. Virtual and specialty pharmaceutical companies are particularly well-suited to CDMO partnerships, and big pharmaceutical companies are beginning to view relationships with CDMOs as strategic rather than tactical.

Working with a CDMO also limits a client’s upfront capital investment for drug development, thus minimizing a project’s cost. By concentrating resources with a single-source provider, the outsourcing client can minimize technical transfer of projects or products, thereby reducing unforeseen costs and potentially speeding new products to market.

Disadvantages of CDMOs

The pharmaceutical client using the services of a CDMO does not have direct control of the project in regard to scheduling, cost, quality or accountability. Security is an issue to be considered when selecting a CDMO, as intellectual property and data are exchanged between client and service provider.

CDMOs

Biovitrum [http://www.biovitrum.com/]
DPT Laboratories, Ltd. [http://www.dptlabs.com/]
Eurogentec [http://biologics.eurogentec.com/]
Glatt Pharmaceutical Services [http://www.glattpharmaceuticals.com/e/00_home/00.htm]

References


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