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OACIB Holiday Schedule 2009
The Office of Animal Care and Institutional Biosafety (OACIB) serving the
Animal Care and Institutional Biosafety Committees (ACC/IBC) will observe
the UIC reduced service schedule for non-essential services beginning on Thursday, December 24th. Therefore, OACIB will close at 5:00 PM on
Wednesday, December 23, 2009, and will reopen at 8:30 AM on Monday, January
4, 2010.
Please remember that the deadline for submission for protocols eligible for
review at the January Meetings is:
- 5:00 PM, Tuesday, December 15, 2009 for
ACC protocols and
- 5:00 PM, Wednesday, December 16, 2009 for IBC
protocols.
In addition, to allow time for the review and approval process
prior to the reduced service schedule, modifications eligible for
administrative or designated review must be submitted by 9 AM on Thursday,
December 17, 2009. |
To download a form:
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Right-click on the format of the form you want to download (e.g., Word,
PDF, etc.)
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Depending on your browser, select Save Target As or Save
Link As.
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Save the file somewhere on your computer where you will remember where
to find it (e.g., C:\My Documents\invention_disclosure.doc).
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Then, open the file from your computer.
If you need any of these forms in MS Word 97, please
email us.
To complete a form:
Use the table below to determine which forms to complete. Then, use these instructions and the UIC IBC Policy as guidelines.
Rules:
- For all research involving animals, appropriate ACC forms must be completed and ACC approval must be obtained prior to beginning work with animals.
- For any research involving a select agent, contact EHSO (312-996-7411) to complete registration requirements. Work may only begin following select agent and IBC approval.
- For all research involving human cells or tissue, bloodborne pathogen training must be completed on an annual basis. Verification of training will be required prior to final IBC approval for personnel listed in Appendix 1 who will be working with human cells or tissue or other bloodborne pathogens. See the education and training schedule.
- For all research involving the shipping or receiving of biological hazards by air, IATA shipping and receiving training must be completed by at least one member of the laboratory listed on Appendix 1. For all research involving shipping or receiving of biological hazards by ground, DOT shipping and receiving training must be completed by at least one member of the laboratory listed on Appendix 1. Please see education and training for additional information.
Tools: Instructions Form A | Instructions Form B | Instructions Form D | BSL1 Manual Template | BSL2 Manual Template
Editing information in IBC
Forms
If your research involves |
Complete |
Work may begin |
Category III rDNA, with all work conducted at BSL1, |
Form A, Appendix 1, & BSL1 Biosafety Manual |
simultaneously with protocol submission. |
Category III rDNA, with at least some work conducted at BSL2 |
Form A, Appendix 1, & BSL2 Biosafety Manual |
following IBC approval. |
Category II rDNA, with all work conducted at BSL1, |
Form A, Appendix 1, & BSL1 Biosafety Manual |
following IBC approval. |
Category II rDNA, with at least some work conducted at BSL2 |
Form A, Appendix 1, & BSL2 Biosafety Manual |
following IBC approval. |
Category II rDNA, with at least some work conducted at BSL3 |
Form A, Appendix 1, & Contact IBC office for information on BSL3 Biosafety Manual Requirements |
following IBC approval. |
Category I rDNA involving deliberate transfer of a drug resistant trait to microorganisms not known to acquire this trait naturally, if such acquisition could compromise the use of the drug to control disease agent in humans, veterinary medicine or agriculture, |
Form A, Appendix 1, & Contact IBC office for initial determination of Biosafety Level, Biosafety Manual requirements, and for Coordination of submission to OBA |
following NIH Director, RAC and IBC approvals. |
Category I rDNA involving cloning of toxic molecules with LD 50 of less than 100 nanograms per kg of body weight, |
Form A, Appendix 1, & Contact IBC office for initial determination of Biosafety Level, Biosafety Manual requirements, and for Coordination of submission to OBA |
following NIH/OBA and IBC approvals. |
Category I rDNA involving cloning of toxic molecules with LD 50 of greater than 100 nanograms, but less than 100 micrograms per kg of body weight, |
Form A, Appendix 1 & Contact IBC office for initial determination of Biosafety Level, Biosafety Manual requirements, and for Coordination of submission to OBA |
following NIH/OBA and IBC approvals. |
Category I rDNA involving deliberate transfer of recombinant DNA, or DNA or RNA derived from recombinant DNA into one or more human subjects, |
Form D & Appendix 1 |
following NIH/OBA, RAC, IRB, and IBC approvals. |
an infectious agent (w/o rDNA), with work conducted at BSL2 |
Form B, Appendix 1, & BSL2 Biosafety Manual |
following IBC approval. |
a toxin, with work conducted at BSL2 |
Form B, Appendix 1, & BSL2 Biosafety Manual |
following IBC approval. |
an infectious agent (w/o rDNA), with work conducted at BSL3 |
Form B, Appendix 1, & Contact IBC office for information on BSL3 Biosafety Manual Requirements |
following IBC approval. |
a toxin, with work conducted at BSL3 |
Form B, Appendix 1, & Contact IBC office for information on BSL3 Biosafety Manual Requirements |
following IBC approval. |
Modifications to previously approved rDNA/IA work |
Form C |
following IBC approval |
Modifications to previously approved rDNA/IA work with human subjects |
Form C |
following IBC and IRB approval |
Human Gene Transfer Event Report |
Form E |
Continue as approved |
Accident/Exposure Event Report |
Form F |
Continue as approved |
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