Research Home > Albany > Albany Research Forms

Reviews Prepatory to Research Associate Chief of Staff for Research Documents Merit Review Albany Research Institute Documents Research & Development Committee Documents Institutional Review Board (IRB) Documents Subcommittee on Research Safety & Biosafety (SRS&B) Security Institutional Animal Care and Use Committee (IACUC) Can't find what you were looking for? Request documents or forms to be e-mailed directly to your inbox!

Reviews Prepatory to Research Reviews Prepatory to Research.doc

Memos From the ACOS ARI-Memo.doc Consent-HIPAA.doc Credentialing.doc EMR-August 8 2006.doc Policy on re-opening a closed study-6-13-06.doc Posting Research Participant Enrollment Note in EMR.pdf ProtocolBrokers-June-2005.doc Security of Data and Remote off-stie storage 6-6-06.doc Study Site Monitor Visits.doc

Merit Review 10-1313-13.doc 10-1313-3.doc 10-1313-4.doc 10-1313-5.doc 10-1313-5and6.doc 10-1313-6.doc 10-1313-7.doc 10-1313-8.doc Handbook1202-1.pdf

Albany Research Institute (ARI) Memos FHPP Costs.pdf Travel ARI-Travel-Procedures.doc ARI-Travel-Reimbursement-Form.doc ARI-Travel-Request-Form.doc VA-Travel-Request-for-Approval-of-Gifts.doc Policies ARIEmployeeManual.doc Intermittent-Time-Card.doc Policy-Procedures.doc Purchase-Order.doc Time-Form.doc

Research and Development (R&D) Information Memo RD Committee.doc R-D Primary Reviewer Form.doc R D Roster.doc RD Meeting Schedule.doc RD SOP Final.doc Forms Amendment Form.doc Change in Investigator Status.doc Checklist JIT 10-28-05.doc Continuing Review Application.doc New Investigator Data Sheet.doc New Investigator Data Sheet Codes.doc Review Form Abstract October 03.doc Review Form Manuscript October 03.doc Review Form Presenta October 03.doc Guidelines & Regulations Consent-HIPAA.doc Data Security Plan Policy.doc Guidelines for Research Protocol.doc MeSH Terms.doc Publications.pdf R D Handbook.pdf RDIS Abstract Guidelines.doc Research Misconduct.pdf

Institutional Review Board (IRB) Information Albanyamendment4Reviewer.doc IRB Meeting Schedule.doc Mandatory HRPP Training Link.doc Member Roster.doc Primary Reviewer Form Initial and Continuing Review.doc Primary Reviewer Reference Guide.doc Forms Amendment Form.doc Application to Undertake Research Involving Human Subjects.doc Conflict of Interest Form.doc Continuing Review Application.doc Cover Page.doc FDA IND Application Instructions.doc FDA Investigational New Drug Application.doc FDA Investigator Agreement.doc Funding Admin Codes.doc HIMS form (blank).pdf IDMC Screening Tool.DOC Imaging Support Letter.doc Informed Consent Template.doc Investigator Agreement Form.doc Lab Support Letter.doc New Protocol Submission Checklist Human Revised.doc Pharmacy Support Letter.doc Request to Review Research Proposal.doc Request to Review Research Proposal II.doc SAE Reporting Form.doc Scope of Practice.doc VA Investigational Drug Record.doc Guides 21 CFR 814.doc 21 FDA 312.doc 21 FDA 50.doc 21 FDA 56.doc 21 FDA 812.doc 38 CFR 17.doc 45 CFR 46.doc Belmont Report.doc Code of Nuremberg.doc VHA Handbook 1058-2 Research Misconduct.pdf VHA Handbook 1200-5.pdf HIPAA HIPAA Attachment A.doc HIPAA Attachment B.doc HIPAA Authorization Withdrawal Form.doc HIPAA Mandate.doc Policies Consent-HIPAA.doc Credentialing Process and Scope of Practice.doc Essential Documents Clinical.doc Institutional Review Board.doc International Research.pdf Standard Operating Procedures Human Research Protection Program HRPP Overview.doc IRB-000 Control Distribution of IRB Standard Operating Procedures.doc IRB-001 Initial Revew of Research.doc IRB-002 Continuing Review of Research Revision.doc IRB-003 Suspension and Termination of Approved Research.doc IRB-004-Study Closure.doc IRB-005 Research Involving Vulnerable Populations.doc IRB-006 Amendments.doc IRB-007 IRB Record Keeping.doc IRB-008 Reporting of Adverse Events and Unanticipated Risks to Subjects and Others.doc IRB-009-Conflict of Interest.doc IRB-010 Consent Process.doc IRB-011-Mandatory Training.doc IRB-012 Membership and Management.doc IRB-013 Advertising and Recruitment of Subjects.doc IRB-014 Protocol Deviations.doc IRB-015 Emergency Use of an Investigational Drug or Biologic.doc IRB-016-IRB Review of Research.doc IRB-017 Outreach Program for Human Research Subjects.doc IRB-018-Sponsored Research.doc IRB-019 Privacy of Research Subjects and Confidentiality of Data.doc IRB-020-Research Related Complaint and Allegations of Non-Compliance.doc IRB-021 Communication.doc IRB-022 Exempt Review.doc IRB-023 Expedited Review.doc IRB-024 Investigator Responsibilities.doc IRB-025 Impaired Decision-Making Capacity.doc IRB-026 IND IDE and Biologics in Human Research.doc IRB-027 HRPP Policy.doc IRB-APPENDIX A.doc IRB-APPENDIX B.doc

Subcommittee on Research Safety & Biosafety (SRS&B) Information 2008 Meeting Schedule.doc Member Roster.doc SRSB SOP rev10-07.doc Forms Biosafety Checklist.doc VA Biosafety Form.doc Guidelines and Regulations Chemical Hygiene Plan.DOC Control of Hazardous Agents in VA Research Laboratories.pdf Data Security Plan Policy.doc NIH Exempt Criteria for Recombinant DNA Experiments.doc NIH Guidelines Section III.doc

Security Data Security Appendix C and D.doc Data Storage for PIs.xls Security Plan Policy.doc

Institutional Animal Care and Use Committee (IACUC) Information 1-14-08 IACUC SOP.doc 2007 Meeting Dates.doc 2008 Meeting Dates.doc ARF SOP October 2007.doc IACUC Member Roster.doc Forms ACORP Appendix I.doc ACORP Appendix II.doc ACORP Appendix III.doc ACORP Appendix IV.doc ACORP Appendix IX.doc ACORP Appendix V.doc ACORP Appendix VI.doc ACORP Appendix VII.doc ACORP Appendix VIII.doc ACORP Main Body.doc Amendment Form.doc Animal PI Checklist.doc Animal Products Form.doc Annual Continued Review Animal Science Research.doc IACUC Submission Checklist.doc IACUCAmendment Checklist.doc Initial Application Animal Science Research.doc Submission Manuscript Jan08.doc Guidelines and Regulations Handbook Use of Animals in Research.pdf

VISN 2 Home | Sitemap | Alphabetical Site Index | What's New | Subscribe | Contact Us | Plug-ins