The purpose of this contract is to provide effective management of these
functions for the BRMP. The contractor shall be responsible for receipt,
dispensing, storage, distribution and inventory control of biologic agents.
Quality assurance and control evaluation which involves specific assays for
sterility, pyrogenicity, endotoxin levels, general safety testing and
preclinical studies related to safe dose and route of administration. The
contractor shall be responsible for processing, vialing, labelling, potency
and purity testing of biologics obtained in bulk form for clinical use. In
some instances production and initial purification of biologics, such as
monoclonal antibodies for clinical trails is performed.
No Sub Projects information available for N01CM073710-007
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for N01CM073710-007
Patents
No Patents information available for N01CM073710-007
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for N01CM073710-007
Clinical Studies
No Clinical Studies information available for N01CM073710-007
News and More
Related News Releases
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History
No Historical information available for N01CM073710-007
Similar Projects
No Similar Projects information available for N01CM073710-007