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Postal codes: USA: 81657, Canada: T5A 0A7

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What does OODP stand for?

Office of Oncology Drug Products (US FDA)


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This definition appears very rarely and is found in the following Acronym Finder categories:

  • Military and Government
  • Science, medicine, engineering, etc.

See other meanings of OODP

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Link/Page Citation...

<< PreviousAbbreviation Database SurferNext >>
Out of Doors Experience
Owners, Officers, Directors, Partners, Regents, Trustees, or Executive Personnel
Object Oriented Design Heuristic(s)
Object Orientated Dynamic Language
Object-Oriented Data Model
Object-Oriented Design Method (programming)
Object Oriented Data Manipulation Language
Object-Oriented Database Management System (also seen as ODBMS)
Object Oriented Design Pattern
Oddhobby Open Directory Project (website)
Ontario Organizational Development Program (est. 1995; Canada)
Opolski Osrodek Doradztwa Rolniczego (Polish)
Optical-Optical Double Resonance
Workshop on Object-Oriented Database Systems
Object Oriented Data Technology
Old Orlu Divisional Union (UK)
Object-Oriented Data Warehouse
Object-Oriented Data Warehouse Design
Object-Oriented Encapsulation
Obligatory Office Equipment



Samples in periodicals archive:
htm FDA Office of Oncology Drug Products http://www.
At last month's ODAC meeting, Richard Pazdur, director of the FDA's Office of Oncology Drug Products, scolded CTI for submitting an incomplete, single pivotal Phase III trial as the basis for its initial submission of the pixantrone application.
Food and Drug Administration's (FDA) Office of Oncology Drug Products has issued a complete response letter regarding the new drug application for OMAPRO(TM) for the treatment of adults with chronic myeloid leukemia who have failed prior therapy with imatinib and have the Bcr-Abl T315I mutation.
director of the FDA's Office of Oncology Drug Products, said during a press briefing after the meeting concluded.
Richard Pazdur, who heads the FDA's Office of Oncology Drug Products, sabotaged Dendreon's application in order to stake his turf as czar of all cancer-therapy approvals.
Food and Drug Administration's (FDA) Office of Oncology Drug Products has issued a complete response letter regarding the new drug application (NDA) for OMAPRO[TM] (omacetaxine mepesuccinate) for the treatment of adults with chronic myeloid leukemia (CML) who have failed prior therapy with imatinib and have the Bcr-Abl T315I mutation.
Approval is not the only pathway to drug access," said Richard Pazdur, director of the FDA's Office of Oncology Drug Products.
Food and Drug Administration's Office of Oncology Drug Products approved more than 50 new indications for the use of oncology and hematology drugs and biologics between July 2005, when the office began reviewing marketing applications, and the end of 2007, according to a new agency study.

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