Radioactive materials ("radioisotopes") for laboratory research
The use of radioactive materials is subject to the terms and conditions
of a radioactive materials license which is issued by the regulatory
agency and held in the Radiation Safety Office. The Radiation Safety
Department monitors and controls the acquisition and use of radioactive
materials and the generation of wastes to ensure that materials
are being used in accordance with the license. Radioactive materials
may only be used for laboratory research purposes if a radioactive
materials "permit" has been issued by the Radiation Safety Office.
Permits are issued to members of the Faculty with appropriate training
and experience, and authorize the use of specific quantities of
specific radioisotopes in specific locations for specific purposes
under specific conditions. The "permit holder" is responsible for
overall supervision and compliance with the terms of the permit,
or for applying for an amendment to the permit. The Radiation Safety
Officer will review the facilities where the material will be used
to ensure adequacy of shielding and ventilation. Approval of research
protocols which involve animals is coordinated with the animal research
oversight committee with jurisdiction at the specific location where
the material will be used. The Radiation Safety Department will
also audit each laboratory to verify compliance with the terms of
each permit and other conditions. Download
a permit application form here
Contact: Lisa Moore or Robert McClosky for further information.
Radioactive materials ("radioisotopes") for clinical diagnosis, therapy or research:
Radioactive materials may only be used for "human use" purposes (clinical diagnosis, therapy or research) if this has been specifically approved by the Medical Isotopes Subcommittee (MIC) of the Radiation Safety Committee of the Tisch Hospital and Bellevue Hospital Medical Boards, and is only permitted within the associated facilities. There are regulatory restrictions on the qualifications and training of physicians and others who may use radioactive materials for human use purposes. The Radiation Safety Office will advise on each situation and acts as the interface to the various committees. Human research protocols which are submitted to the IBRA for approval are forwarded to the Radiation Safety Office for the additional step of MIC approval. The Radiation Safety Department has the same oversight and auditing role as for laboratory research, but it also supervises the preparation and use of rooms where radioactive materials are used for therapeutic purposes, ensures adequacy of shielding, provides safety support and instruction to the nursing staff, and determines when patients may be released from special precautions as required to ensure safety and regulatory compliance.
Contact: Steven Wagner for further information on the human use of radioactive materials.
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