§ 100003. Conflicts of Interest -- Non-ICOC Members of the Scientific and Medical Research Fund...
17 CA ADC § 100003Barclays Official California Code of Regulations
17 CCR § 100003
§ 100003. Conflicts of Interest -- Non-ICOC Members of the Scientific and Medical Research Funding Working Group (the “Grants Working Group”).
(a) Prohibition: Except as provided otherwise in this regulation, a non-ICOC Grants Working Group member may not participate in a decision of the working group in which the individual has a conflict of interest. A conflict of interest exists when a non-ICOC Grants Working Group member has a real or apparent interest in the outcome of an application such that the member is in a position to gain financially, professionally or personally from either a positive or negative evaluation of the grant proposal.
(1) The member or a member of his or her Immediate Family is an employee of either the applicant organization, a Subcontractor, or a Partner, or has received, or has been promised, income or anything else of value, of $5,000 or more, or gifts worth $500 or more, in the past year from the applicant institution, a Subcontractor, a Partner, or a person listed in the application as Key Personnel.
(4) A member or a member of his or her Immediate Family has a financial interest in the organization, a Subcontractor, or a Partner of $5,000 or more. A “financial interest” includes current stock holdings, equity interest, intellectual property or real property interest, but does not include an interest held through a diversified mutual fund.
(f) Disqualification: A non-ICOC member is required to report to the CIRM staff any conflict of interest of which he or she is aware, including, but not limited to, those described in subdivisions (b) through (e) of this regulation, and any application as to which the Member believes his or her objectivity could be compromised. A non-ICOC member of the Grants Working Group who has a conflict of interest, as described in subdivisions (b) through (d) of this regulation, or who believes that his or her objectivity could be compromised with respect to an application may not review or vote on the application and must leave the room when that application is discussed. In exceptional cases, the President of the CIRM may decide that the need for special expertise of the reviewer outweighs any possible bias posed by a real or apparent conflict of interest. Under these circumstances, the CIRM staff shall publicly disclose the working group member's interest before the meeting and the working group member shall be permitted to participate in the discussion but will not be permitted to vote on the application or participate in the scientific scoring.
(g) All non-ICOC members must indicate any possible conflicts of interest that they have in advance of a review and must certify that they did not participate in the discussion or review of any application for which they have a conflict of interest, or indicate permission to participate was granted by the President pursuant to subdivision (f) of this regulation.
(h) Record-Keeping: All financial disclosure documents shall be kept confidential by the CIRM staff and preserved for purposes of review by the State Auditor or another independent auditor and any other audit as required by law. Records of the working group indicating those members who participated in or voted on particular recommendations shall be maintained by the CIRM staff. If the CIRM or an auditor discovers a violation of these conflict of interest provisions, a report will be made to the Legislature along with a review of corrective actions taken by the CIRM to prevent future occurrences.
(2) “Key Personnel” means (i) the principal investigator or program director; or (ii) any other person, including an independent consultant or an employee of a Subcontractor or Partner, who is expected to contribute to the scientific development or execution of the project in a substantive, measurable way and who is expected to: (a) receive or has been promised income, or anything else of value, of $10,000 or more per year through the proposed project or (b) contribute one percent (1%) or more effort to the proposed project. “Key Personnel” does not include a person who is expected to be involved in the proposed project but who does not satisfy paragraphs (i) or (ii).
(3) “Partner” means an organization that, in exchange for the right to the opportunity for a future financial return, has agreed to provide matching funds for the proposed project or entered into an agreement with the applicant organization relating to the commercialization of the proposed project. Partner does not include an organization that, like the National Institutes of Health, provides research funding to a proposed project but that does not have the right to a future financial return.
(4) “Research Collaborator” or “Research Collaboration” means participation as Key Personnel on the same research project or effort to advance or publish research results or the commercial development of a product. The terms do not include passive associations such as belonging to the same scientific society or contributing to the same review article or textbook.
(5) “Subcontractor” means an organization (other than the applicant organization) that is expected to: (a) contribute to the scientific development or execution of the project in a substantive, measurable way and (b) receive $25,000 or more through the proposed project. “Subcontractor” does not include suppliers of widely available goods.
Credits
Note: Authority cited: California Constitution, article XXXV; Section 125290.40(j), Health and Safety Code. Reference: Sections 125290.50(e) and 125290.60, Health and Safety Code.
History
1. New section filed 10-5-2006; operative 11-4-2006 (Register 2006, No. 40).
2. Amendment filed 1-21-2016; operative 4-1-2016 (Register 2016, No. 4).
This database is current through 4/12/24 Register 2024, No. 15.
Cal. Admin. Code tit. 17, § 100003, 17 CA ADC § 100003
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