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Virginia Tech
Governance Minutes ArchiveOctober 11, 1989
Minutes COMMISSION ON RESEARCH October 11, 1989 President's Board Room 3:30 p.m. MEMBERS PRESENT: L. J. Arnold, F. M. Asche, D. M. Denbow, V. R. Fu, P. L. Knox, J. C. Lee, C. McDaniel (for G. E. Bunce), J. Randolph, R. S. Russell, E. R. Stout, W. L. Stutzman MEMBERS ABSENT: W. L. Flowers, E. G. Henneke, G. R. Hooper, W. G. Huber, M. Potts, M. G. Squires, H. H. Stoevener, L. A. Swiger INVITED GUESTS: M. D. Shelton 1. Dr. Stout announced our Director of Sponsored Programs, Dorothy Richardson, died on September 29th. The EEO/AA Office has been con- tacted. Whether the search can be resumed at the point Dorothy was hired or whether we have to initiate a new search remains to be seen. Dr. Stout is Acting Director of Sponsored Programs. 2. The Commonwealth Center in Interdisciplinary Mathematics has been re- commended by the State Council. 3. Adoption of Agenda with suggested addition by Dr. Arnold of certif- ication of human subjects. Agenda was approved. 4. Approval of Minutes of September 13 with correction of Virginia "Prin- ciples" Assessment Center to Virginia "Principals" Assessment Center. 5. Interdisciplinary Research Committee. The Chairman suggested that the Committee be composed of 2 college faculty representatives, 1 Faculty Senate representative, 1 department/division representative, and 1 cen- ter director. Dr. Arnold wanted standard statement of purpose. Dr. Stout stated that by next committee meeting he would have statement of purpose and suggested membership. Dr. Randolph suggested the Commis- sion might consider a committee dealing with core research. Dr. Randolph agreed to bring back recommendation concerning core research committee. 6. NIH final rule on misconduct in science was published in the Federal Register in late September. Presidential Policy Memorandum #102 fac- ulty ethics - whether present statement covers us as far as NIH we don't know. Kay Heidbreder, Assistant Legal Counsel, is checking into it and hopefully will be able to provide us with an opinion next meet- ing. Dr. Stout stated he was confident that our statement was inade- quate in one respect that in our statement there is nothing about reporting procedures to sponsors. NIH wants a mechanism to deal with it and a mechanism to report back to them. Dr. Arnold suggested the Commission draft a policy for the Faculty Senate or Commission on Fac- ulty Affairs. Policy starts November 8 pertaining to grants and not contracts. If our policy in place is determined to be inadequate, Dr. Stout will write a cover letter stating we have a policy, we've been advised it is inadequate and we're working on it. 7. Certification - procurement integrity. Once procurement announcement is published, then no one at institution can have any contact with any- one at the agency who has anything to do with that program. The uni- versity has to certify that procurement regulations have been followed. Only applies to Department of Defense procurements including research contracts. 8. Dr. Stout reviewed the handouts sent - commentary from the Chronicle of Higher Education, October 4, and Trends in the South. 9. DHHS certification of Institutional Review Boards for Research Involv- ing Human Subjects: Dr. Arnold asked: What's necessary to be certi- fied and what does it mean to be certified and if it saves us time shouldn't we go ahead and get certification? Dr. Stout responded: Many institutions, especially medical schools have "broad assurance" from NIH. Such institutions are assigned an "assurance number". When a proposal is sent to a Federal agency that involves the use of human subjects, a form (HHS 596) must accompany it. One section of the form is "HHS Assurance Status". If an approved assurance of compliance is on file with DHHS which covers the activity in the proposal, the assur- ance number is entered. Alternatively, the "single assurance" box is checked. Any proposal that has the "human subjects" question checked on the back of the Proposal Internal Approval Form is sent to the Chairman of the IRB (Dr. Stout). He then writes to the P.I. requesting that approval of the research protocol, consent forms, etc. be secured from the department. Dr. Stout may give expedited approval on behalf of the IRB or call a meeting of the IRB to review and approve the re- search. Dr. Stout then sends an amended HHS 596 to the sponsor. Dr. Stout has contacted the Office of Protection of Research Risks (OPRR) at NIH and has been advised that without a medical school seeking broad assurance certification is not warranted. 10. Meeting adjourned at 4:35PM. ERS/php
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