CIRM Stem Cell Grant Regulations
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CIRM Regulations
- [100000] – Conflict of Interest Code – CIRM
- [100001] – Definitions for Working Group Conflict of Interest Provisions
- [100002] – Conflicts of Interest – Non-ICOC Members of the Scientific and Medical Accountability Standards Working Group
- [100003] – Conflicts of Interest – Non-ICOC Members of the Scientific and Medical Research Funding Working Group
- [100004] – Conflicts of Interest – Non-ICOC Members of the Scientific and Medical Facilities Working Group
- [100005] – Conflicts of Interest – Members of Advisory Task Forces
- [100010] – Scope of Chapter 2 – Stem Cell Research
- [100020] – Definitions
- [100030] – Activities Not Eligible for CIRM Funding
- [100040] – Institutional Assurance of Compliance
- [100050] – Compliance
- [100060] – SCRO Committee Membership and Function
- [100070] – SCRO Committee Review and Notification
- [100080] – Acceptable Research Materials
- [100081] – Exemption Petition for Lines Derived Prior to November 22, 2006
- [100085] – Use of Fetal Tissue
- [100090] – Additional Requirements for CIRM-Funded Derivation
- [100095] – Additional Requirements for CIRM-Funded Research Involving Oocytes
- [100100] – Informed Consent Requirements
- [100110] – Fairness and Diversity in Research
- [100120] – Record Keeping
- [100300] – Intellectual Property Requirements for Non-Profit Organizations – Scope
- [100301] – Intellectual Property Regulations – Definitions
- [100302] – Invention Reporting Requirements
- [100303] – Publication Requirements
- [100303] – Publication Requirements – effective July 1, 2013
- [100304] – Biomedical Materials
- [100305] – Patent Applications
- [100306] – Licensing CIRM-Funded Patented Inventions
- 100307 – [Reserved]
- [100308] – Revenue Sharing
- [100309] – Press Release Requirements
- [100310] – March-In Rights
- [100400] – Intellectual Property and Revenue Sharing Requirements for For-Profit Organizations – Scope
- [100401] – Intellectual Property Regulations – Definitions
- [100402] – Invention and Licensing Reporting Requirements
- [100403] – Publication Requirements
- [100403] – Publication Requirements – Effective July 1, 2013
- [100404] – Publication-Related Biomedical Materials Requirements
- [100405] – Patents
- [100406] – Licensing CIRM-Funded Patented Inventions
- [100407] – Access Requirements for Products Developed by For-Profit Grantees
- [100408] – Revenue Sharing
- [100409] – Press Release Requirements
- [100410] – March-In Rights
- [100500] – Grants Administration Policy for Academic and Non-Profit Institutions (for grants made on or after November 2, 2012)
- [100500] – Grants Administration Policy for Academic and Non-Profit Institutions (for grants made prior to November 2, 2012)
- [100501] – Grants Administration Policy for For-Profit Organizations (for grants made prior to May 21, 2016)
- [100502] – Definition of California Supplier
Authority to adopt regulations
Health & Safety Code Section 125290.40, subdivision (j), permits the ICOC to adopt, amend and rescind rules and regulations to carry out the purposes and provisions of Proposition 71 (“Act”) and to govern the procedures of the ICOC. Properly adopted regulations carry the same force and effect as law.
Types of Regulations
The Act provides two methods for the ICOC to adopt regulations – either “Interim” regulations or permanent regulations adopted pursuant to the California Administrative Procedures Act (“APA”).
Prop 71 Interim Regulations
The ICOC may adopt interim regulations exempted from compliance with the procedures set forth in the APA. The interim regulations are adopted by the ICOC and remain in effect for 270 days unless earlier superseded by regulations adopted pursuant to the APA. (125290.40, subd. (k).) Not every regulation adopted by the ICOC will be preceded by an “interim” version (see below).
Formal APA Regulations
The ICOC may also adopt regulations pursuant to procedures described in the APA in the same manner as other state agencies. Unless otherwise provided in the regulations themselves, these regulations remain in effect indefinitely or until they are repealed or amended by the ICOC in procedures established by the office of Administrative Law, the agency that implements the APA. (These procedures are described at the OAL website: www.oal.ca.gov.)
The ICOC will approve a draft policy or regulation(s) for submission to the OAL to begin the regulation adoption process. Staff will place the policy or draft regulations in proper form and will make a formal submission to the OAL, called the “OAL Notice.” Links to both documents (when completed) can be found in the chart below.
Except in the case of interim and emergency regulations, the APA establishes a formal rulemaking process which includes a minimum 45 day public-comment period. During that period, comments may be submitted to the CIRM in response to the proposed regulation.
How to submit public comments
You may submit written statements, arguments, or comments relating to the proposed regulation in writing to the CIRM during the comment period specified for each regulation. Comments may be submitted electronically to the address indicated, mailed to:
CIRM Proposed Rulemaking
[indicate the specific proposed regulation, e.g., Conflict of Interest Code]
601 Gateway Blvd. Suite 400
South San Francisco, CA 94080
Consideration of public comment
The CIRM will consider all relevant material it receives during a Noticed opportunity to comment before adopting, amending, or repealing any regulation, including comments received via FAX and email. (Govt. Code §§11346.8, subd. (a); 11340.8, subd. (a).) Responses to comments received during the public comment period will be provided in the final statement of reasons submitted to the office of Administrative Law along with any modifications made to the proposed regulation responsive to the public comments received.
