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Information and Guidance on the new NIH Public Access Policy |
| 21 CFR 11 Compliance Memo | Data System Compliance Memo providing information on compliance with federal regulations of our three primary clinical information systems: Access Anywhere, Practice Partner and Oacis. Questions regarding this memo can be addressed to Reece Smith at 792-7795. |
Clinical Trials Registration |
New Law requires expanded registation of clinical trials in the ClinicalTrials.gov protocol registration system. For information and instructions on the registration of your clinical trial, see our Information Sheet. Additional information can be found in the NIH Notice NOT-OD-08-014 |
| New Cayuse software to prepare grants.gov applications | |
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Training Sessions for Cayuse Grants.gov submissions |
| Policy for reimbursement for tuition and fees for fulltime PhD Students | |
| Export Controls | |
| NIH News and Updates | |
On Line Training
in Research and Sponsored Programs Issues. |
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MUSC Policy for Research Administration |
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In the case of a researcher knowingly omitting industry funding
information from an NIH grant application, the U.S. Court of appeals
held both the researcher and the institution liable under the federal
False Claims Act. [US ex rel Catekin v. Univ. of Pittburgh] The false Claims Act imposes liability for treble damages against anyone who knowingly submits a false statement to the government in an effort to obtain federal funds. |
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Reminder... Final technical and invention reports are due 90 days after termination of the project. Failure to report may jeopardize future funding from the sponsor. |
Last
modified on May 2, 2008
