To initiate review of a protocol by the GESCR Committee (and the IRB if necessary), submit an application through iRIS, our electronic submission system. To submit in iRIS, please follow these instructions.

The applicant makes an initial determination whether GESCR and/or IRB review are required; the final determination is made by the GESCR staff or Chair. The level of GESCR review is determined by the GESCR staff, Chair and reviewers.  

On receipt of the application, the GESCR Coordinator:

1. Screens the information provided
2. Requests any changes needed from the researchers
3. Forwards the application to the GESCR Committee Chair/designated reviewer or GESCR Committee
4. Forwards any additional requests for changes to the researchers
5. Processes approval once all changes are addressed and the Chair/Committee approves the study

Additional Information: At any stage in the review process, the Chair or lead reviewer may require the applicant to submit additional information or documentation to the GESCR Committee in support of the Application.

Additional Review: If the Chair determines, at the Chair’s discretion, that a protocol requires an additional review, he or she may forward the Application to an ad hoc reviewer or to one or more additional Committee members for additional review on an expedited basis or to the full review.

If the Chair or designated reviewer determines that a protocol that is undergoing an expedited review (minimal concern or scientific) raises concerns about transferring human characteristics to non-human animals, he or she must forward the Application to the Committee for full review.

Additional Approval: Work may not begin on a protocol approved by the GESCR Committee until all other requirements have been met, including approval by the IRB, the Institutional Animal Care and Use Committee (IACUC) or the Biologic Safety Committee, as needed.

GESCR approvals are issued for one year. You may not conduct any research activity after the expiration date. GESCR requires an application for continuing review prior to the expiration date in order to review and renew a protocol.

When do I submit my Continuing Review?

We advise that researchers submit their renewals 6 -12 weeks before the expiration date.  Studies involving human subjects (tissue sampling – clinical trials) will take longer to review than protocols without human subjects (protocols such as in-vitro only or simple animal testing projects) because they will need to be reviewed by both the GESCR and IRB Committees.

1. Change of personnel named in the Application*
2. Change in office or laboratory site - within the UCSF campuses
3. Minor corrections or clarifications to the study documents

*Change of PI should be reviewed as an Expedited/Minimal Concern submission.

A. Protocols involving purely in vitro research, excluding protocols for differentiation of human stem cells into gametes or totipotent cells, which use only:

1. Human adult stem cells or human cord blood stem cells

2. Human pluripotent stem cell lines that have been “acceptably derived”. For purposes of this document, pluripotent stem cell lines have been “acceptably derived” when they have been:

a. Approved by the National Institutes of Health (NIH)

b. Deposited in the United Kingdom Stem Cell Bank

c. Derived by, or approved use by, a licensee of the United Kingdom Human Fertilization and Embryology Authority

d. Derived in accordance with the Canadian Institutes of Health Research Guidelines for Human Pluripotent Stem Cell Research under an application approved by the National Stem Cell Oversight Committee

e. Derived in accordance with the Japanese Guidelines for Derivation and Utilization of Human Embryonic Stem Cells

f. Found to be “acceptably derived” by the California Institute for Regenerative Medicine

3. Human stem cell lines which have previously been approved for use by the GESCR Committee unless there is new information that calls into question renewal or approval 

4. Non-pluripotent human stem cells derived from a stem cell line listed in Section II.A.1, 2 or 3 (above)

5. Induced pluripotent stem (iPS) cells, excluding research directed at creating a totipotent human cell from an iPS cell, which satisfy at least one of the following requirements:

a. The GESCR Committee approved the consent form and process for obtaining the somatic cells used for induction

b. The GESCR Committee receives written confirmation from a Stem Cell Oversight Committee, an Institutional (IRB); or, if the iPS cells were derived at an institution outside of the United States, a substantially equivalent oversight body, that the oversight body approved the process for obtaining the somatic cells used for induction

c. The process for obtaining the somatic cells used for induction was not “research involving human subjects” within the meaning of Title 45, Part 46 of the US Code of Federal Regulations (45 CFR Part 46)

d. The process for obtaining the somatic cells used for induction was exempt from the requirements of 45 CFR Part 46, under 45 CFR Part 46.101(b)

B. Protocols for human iPS cell induction, where the process for obtaining the somatic cells used for induction satisfies the requirements of Section II.A.5 above.

C. Protocols involving the injection/transplantation of human cells into post-natal non-human animals, which use a stem cell line that is described in Section II.A above, excluding:

1. Protocols involving the introduction of neural progenitor cells into the brains of post-natal non-human animals

2. Protocols involving the introduction of human pluripotent stem cells into post-natal non-human animals, except for teratoma formation to verify pluripotency

3. Protocols in which there is a significant possibility that the implanted stem cells could give rise to functional neural or gametic cells and tissues. In considering the likelihood of such an outcome, particular attention should be paid to at least three factors              

a. The extent to which the implanted cells colonize and integrate into the animal tissue

b. The degree of differentiation of the implanted cells

c. The possible effects of the implanted cells on the function of the animal tissue

D. Protocols involving the use of human oocytes or embryos that are inadequate for reproductive purposes, would otherwise be discarded and will not be used to create pluripotent stem cells

E. Continuing Reviews (renewals) of approvals for protocols and requests for modifications to protocols which have been previously approved by the GESCR Committee, where no modifications to the protocol require Expedited/Scientific review or Full Review, regardless of the initial level of review.

A. Protocols involving the injection of human stem cells into non-human blastocysts, embryos or fetuses, which use a stem cell line that is described in Section II.A, above, excluding:

1. Protocols involving the introduction of human pluripotent stem cells into non-human blastocysts, embryos or fetuses

2. Protocols involving the introduction of neural progenitor cells into non-human blastocysts, embryos or fetuses

3. Protocols in which there is a significant possibility that the implanted human stem cells could give rise to functional neural or gametic cells and tissues.  In considering the likelihood of such an outcome, particular attention should be paid to at least the three factors listed in Section II.C.3 

B. Protocols involving the injection of human stem cells into non-human post natal animals that:

1. Use a stem cell line that is described in Section II.A, above

2. Do not qualify for Expedited/Minimal Concern review under Section II.C.3

But excluding:

a. protocols involving the introduction of human pluripotent stem cells into post-natal non-human primates

b. protocols involving the introduction of neural progenitor cells into the brains of post-natal non-human animals