Research Compliance. If you have an active research collaboration with the partner institution, please complete the following information. Name of primary faculty collaborator abroad: Will a translation of this agreement be needed? Yes No Is this research already linked to a NU Grant Project? Yes No If yes: please provide the project number or form number. By signing below I am acknowledging my request to renew an international agreement and I agree to work with the International Engagement Office to keep them informed of my efforts abroad. International Engagement Office, Love Library South 000, Xxxxxxx, XX 00000-0000
Research Compliance. The Supplier shall deploy research techniques that comply with the principles set out within the European Data Protection Regulations and specifically the The General Data Protection Regulation (GDPR) (Regulation (EU) 2016/679). See Section 25: Qwarie Compliance Statement
Research Compliance. Does this research use: Recombinant DNA? If “Yes,” IBC approval will be required before an award can be made. Human Subjects? If “Yes,” IRB approval will be required before an award can be made. Vertebrate Animals? If yes, IACUC approval will be required before an award can be made. CITI Training? If yes, expiration date / / . Yes No Yes No Yes No Yes No COI Completion If yes, expiration date / / . Yes No If an award is made, the recipient will abide by all guidelines established by the Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and/or the Institutional Biosafety Committee (IBC) and any other relevant University Compliance committee reviews or institutional requirements, in addition to any cooperative agreements between the University and other institutions. Signature of Principal Investigator Date _ _ _ _ Signature of Principal Investigator’s Supervisor Date _ _ _ _ _ Print or type name of Principal Investigator’s Supervisor Date Signature of Department Chair Date /Principal Investigator (Last, First, Middle): SENIOR/KEY PERSONNEL. See instructions. Use continuation pages as needed to provide the required information in the format shown below. Start with Program Director(s)/Principal Investigator(s). List all other senior/key personnel in alphabetical order, last name first. Name eRA Commons User Name Organization Role on Project OTHER SIGNIFICANT CONTRIBUTORS Name Organization Role on Project PROJECT/PERFORMANCE SITE(S) (if additional space is needed, use Project/Performance Site Format Page) Project/Performance Site Primary Location Location: Street: Street 2: City: County: State: Project/Performance Site: Additional Project/Performance Site Location Name: Street: Street 2: City: County: State: SPIRE Need for Funding Principal Investigator: Title of Proposal: _ Form must be typewritten. If more space is needed, please use one additional page for each section.
Research Compliance. The SUBRECIPIENT certifies by signature to this Agreement that the research project will comply with all Research Compliance and obtain all necessary approvals for Human Subjects, Vertebrate Animals, Recombinant DNA and any other areas that require protocol review. 8.
Research Compliance. AWARDEE shall perform the research in compliance with all INSTITUTION policies, and applicable state and federal laws and regulations. ACADEMY assumes no responsibility for AWARDEE’s performance of the RESEARCH. INSTITUTION and AWARDEE agrees to conduct RESEARCH and maintain records and data during and after the term of this Agreement in compliance with all applicable legal and regulatory requirements, including without limitation, any applicable requirements of the Food and Drug Administration.
Research Compliance. DSH is a covered entity under the Health Insurance Portability and Accountability Act of 1996 (HIPAA). DSH may receive protected health information and patient identifying substance use disorder treatment information for research purposes so long as disclosure is consistent with federal and state laws. Without limiting the generality of the foregoing, in accordance with 42 C.F.R. part 2.52(a) and 45 C.F.R. part 164.512(i), Contractor shall only disclose the data to DSH for research purposes after DSH obtains approval from the State of California’s Institutional Review Board, the California Health and Human Services’ Committee for the Protection of Human Subjects and furnishes documentation to Contractor. DSH shall follow all of its internal policies and procedures for obtaining approval for research using data reported by contractor. DSH agrees to comply with HIPAA and 42 C.F.R. Part 2 regarding all requirements including retention and destruction.
Research Compliance. If you've already begun a research collaboration with the proposed partner institution, please complete the following information. Name of primary faculty collaborator abroad: Description of research/collaboration: Will a translation of this agreement be required? If an official translation of this agreement will be required, any professional translation costs will be paid by the partner institution or faculty requestor. Yes No Is this research already linked to a NU Grant Project? Yes No By signing below I am acknowledging my request to submit a proposal for an international agreement and I agree to work with the Global Strategies Office to keep them informed of my efforts abroad. Global Strategies Office, Love Library South 000, Xxxxxxx, XX 00000-0000
Research Compliance. The University will ensure compliance of the Research with Applicable Law and other rules applicable to Research and Research billing including, but not limited to, laws and regulations governing human subjects research, research integrity, conflicts of interest, Medical Center policies and University IRB rules, regulations and policies and grantor requirements. The University shall ensure that Clinical Services are not compromised by Research.
