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core flow training PDF document core flow training Research Facilities
What Research Administration Can Do for YOU PDF document Information about services of research development, sponsored programs office,post award, and research accounting Presentations
Ways to Prepare for a QAIP Study Site Visit Word document Prepare for Site Visit QAIP—Quality Assessment & Improvement Program
Waiver of Authorization Request Formi Word document Form IRB—Institutional Review Board (Human Subject)
Volunteer Recruitment Formi Word document Form IRB—Institutional Review Board (Human Subject)
Using the Clinical Research Unit PDF document Policies and procedures for using the Upstate Medical University Clinical Research Unit Research Facilities
Upstate Research Misconduct Policy Word document Defines research misconduct and explains the process of assessing and invetigating allegations General Research Policies
Upstate Policy on Identification and Management of Conflicts of Interest and Commitment PDF document This policy establishes standards for identification and management of conflicts of interest and commitment in research, education and patient care. General Research Policies
Upstate IRB Guidelines & Policies PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Upstate Financial Disclosure Formi PDF document This form is completed by Upstate faculty, staff and students applying for extramural research funding who will participate in the design, conduct or reporting of the research Research Administration
Upstate Core Facilitites-Proteomics Core PDF document Information regarding research supported by and how to access the Proteomics Core Facility Presentations
Upstate Core Facilities-Musculoskeletal Core PDF document Information about the types of research supported by and how to access teh Musculoskeletal Core Presentations
Upstate Core Facilities-Microarray-Based Research Core PDF document Information regarding the types of research supported by and how to access the Microarray-Based Research Core at Upstate Presentations
Upstate Core Facilities-MRI Research Core PDF document Information regarding research supported by and how to access teh MRI Research Core Presentations
Upstate Core Facilities-In vivo Micro CT Core Laboratory PDF document Provides information about the research supported and how to access the In vivo MicroCT Core Facility Presentations
Upstate Core Facilities-Flow Cytometry Core PDF document Information regarding research supported by and how to access the Core Facility for Flow Cytometry Presentations
Upstate Core Facilities-DNA Sequencing Core PDF document information about research supported by and how to access the Core Facility for DNA Sequencing Presentations
Upstate Core Facilities-Confocal & 2-photon Core PDF document Research supported by and how to access Upstate's Confocal & 2 Photon Core Facility Presentations
Upstate Core Facilities-Clinical Research Unit PDF document Services and capacity of and how to access the Clinical Research Unit at the IHP Presentations
Upstate Core Facilities-Cetner for Humanized SCID Mouse Models & Stem Cell Processing Lab PDF document information regarding research supported by the Center for Humanized SCID mouse models and Stem Cell processing lab Presentations
Upstate Core Facilities-Center for Research and Evaluation (CRE) PDF document Services of and how to access the Center for Research and Evaluation Presentations
Upstate Authorship Policy PDF document This policy is based upon the ICMJE guidelines for granting authorship and contributorship General Research Policies
University Hospital, Voluntary Faculty Request to Conduct Research which Requires the Use / Disclosure of IIHIi PDF document Form IRB—Institutional Review Board (Human Subject)
University Hospital Patient Data Request Form PDF document Form IRB—Institutional Review Board (Human Subject)
Unanticipated Problems and Adverse Event Flow Chart PDF document Determination Flow-chart IRB—Institutional Review Board (Human Subject)
Transporting Biohazardous (including human blood, body fluids and tissue) Items PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
This Week in Research @ Upstate PDF document Highlights of Biomedical Research Seminars for the current week. This Week in Research at Upstate
The Impact of The HIPAA Privacy Rule on Research PDF document Educational Presentation IRB—Institutional Review Board (Human Subject)
Tech Transfer-What Happens After You Invent PDF document Information about turning inventions into assets, protecting and managing asset rights, and turning IP assets into gain Presentations
Tech Transfer-From Discovery to Patent Application Filing...and Beyond PDF document Steps in taking a discovery (invention) from initial disclosure to obtaining a patent and/or license Presentations
Tech Transfer-Find Funding to Commercialize Technology using SBIR & STTR Programs PDF document Information about the SBIR and STTR programs for researchers to find funding to commercialize their discoveries Presentations
Survey of Staff Use of Safety Medical Devicesi Word document Form IBC—Institutional Biosafety Committee
Summary of NIH Guidlines for Research Involving Recombinant DNA Molecules PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
Summary of Guidelines for Research Involving Infectious Agents or Recombinant DNA Molecules PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
Subject Enrollment Logi Word document Enrollment Log QAIP—Quality Assessment & Improvement Program
Subject Eligibility Checklisti Word document Eligibility Checklist QAIP—Quality Assessment & Improvement Program
Study Team Signature and Delegation of Responsibility Logi Word document Responsibility Log QAIP—Quality Assessment & Improvement Program
Study Initiation Visit: Preventive Care for Your Study Site PDF document Education QAIP—Quality Assessment & Improvement Program
Study Initiation Key Points PDF document Key Points include: Informed Consent, Continuing Review Submission to the IRB, Confidentiality and HIPAA Issues, Amendments to Approved Protocols, Adverse Event Reporting to the IRB, Protocol Deviation Reporting to the IRB,DSMB Submission to the IRB QAIP—Quality Assessment & Improvement Program
Student Work/Research Mentor Directory PDF document Student Summer Research List of Mentors and Supervisors Student Research
Strategic Plan: Research Implementation Plan PDF document A detailed series of events required to strengthen and grow our research enterprise. Research Administration
Strategic Plan for Strengthening Research PDF document This plan details SUNY Upstate's four research pillars and is the blueprint for the future. Research Administration
Spanish Lanuage Standard Consent Sections Word document Standard language for the 'In Case of Injury', 'Questions', and 'Voluntary Participation' sections IRB—Institutional Review Board (Human Subject)
Spanish Language Version Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Site Visit Checklist i Word document Checklist IBC—Institutional Biosafety Committee
Signature Authorization Formi PDF document Post Awards document for PI to authorize funds Research Administration
Security of Research Data: How to Protect Research Subjects PDF document Overview of relevant FDA guidelines, HIPAA Security, and State Law; best practices to follow for protecting electronic information IRB—Institutional Review Board (Human Subject)
Sample Assent Form Word document Form IRB—Institutional Review Board (Human Subject)
Safety Product List PDF document List of safety products IBC—Institutional Biosafety Committee
SOP for Obtaining Consent from Subjects who Enrolled as a Minor PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
SOP for Establishing Legal Guardianship for Pediatric Subjects PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Research on Decedent's Information Requesti Word document Form IRB—Institutional Review Board (Human Subject)
Research Strategic Plan Implementation Schedule PDF document Research Strategic Plan Implementation Schedule Research Administration
Research Misconduct Policy PDF document Guidelines/Policies for responding to allegations of research misconduct, updated August, 2011 Research Administration
Research Implementation Plan 2012 Update PDF document Strategic Plan: Research Implementation Plan 2012 Update Research Administration
Research Forum: Issue 41 PDF document Research Forum Newsletter Spring 2011 Research Forum Newsletters
Research Forum: Issue 40 PDF document Research Forum Newsletter Winter 2010-2011 Research Forum Newsletters
Research Forum: Issue 39 PDF document Research Forum Newsletter Fall 2010 Research Forum Newsletters
Research Forum: Issue 38 PDF document Research Forum Newsletter Summer 2010 Research Forum Newsletters
Research Forum: Issue 37 PDF document Research Forum Newsletter Spring 2010 Research Forum Newsletters
Research Forum: Issue 36 PDF document Research Forum Newsletter Winter 2009-2010 Research Forum Newsletters
Research Forum: Issue 35 PDF document Research Forum Newsletter Fall 2009 Research Forum Newsletters
Research Conflict of Interest Committee Membership PDF document Research Conflict of Interest Committee Membership General Research Policies
Research Compliance Reference List PDF document Education QAIP—Quality Assessment & Improvement Program
Research Billing Form Word document Research Billing Form Clinical Trials
Requesting an IND Consult from the FDA PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Requesting Use of CRU Application PDF document Application to request use of the Upstate Medical University Clinical Research Unit Research Facilities
Request for Tissue for Research Purposes (Pathology Department Form)i Word document Form IRB—Institutional Review Board (Human Subject)
Request Exemption from IRB Review PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Reporting of Protocol Deviations PDF document Protocol Deviation Policy IRB—Institutional Review Board (Human Subject)
RF Fringe Benefit Rates PDF document Research Foundation Fringe Benefit Rates Research Administration
QAIP Site Visit Schematic Chart PDF document QAIP Schematic QAIP—Quality Assessment & Improvement Program
QAIP Site Visit Formi Word document Site Visit Form QAIP—Quality Assessment & Improvement Program
QAIP Compliance Tips PDF document Tips and Best Practices QAIP—Quality Assessment & Improvement Program
Proteomics Core Research Facility SERVICES and PRICING PDF document Proteomics Core Research Facility SERVICES and PRICING info Research Facilities
Policy on IRB Review for Studies Pending Funding PDF document Policy IRB—Institutional Review Board (Human Subject)
Policy and Procedures for Research Involving Recombinant DNA, and Infectious or Bio-Hazard Agents (Including Human Gene Transfer Research) PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
Policy and Procedures for Research Involving Human Blood, Fresh Human Tissue, or Body Fluids PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
Pharmacy Service Fees PDF document For use when negotiating a budget for Pharmacy Fees Clinical Trials
Parental Permission Only Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
PHS Policy Promoting Objectivity in Research PDF document Policy establishes standards that provide a reasonable expectation that the design, conduct and reporting of research funded under PHS grants, cooperative agreements or contracts will be free from bias resulting from financial conflict of interest. General Research Policies
New Technology Disclosure (NTD) Procedure PDF document Guidelines Patent/New Technology Transfer
New Technology Disclosure (NTD) Formi Word document Form Patent/New Technology Transfer
New Company Formation PDF document How to Create A New Company Patent/New Technology Transfer
Narrative (notes-to-file) Formi Word document Note-to-File Form QAIP—Quality Assessment & Improvement Program
NIH Public Access-Upstate & the NIH Public Access Policy PDF document information about the NIH Public Access policy and Upstate resources to assist researchers comply with this policy Presentations
NIH Public Access-PubMed, PubMed Central, Open Access, and Public Access PDF document NIH new Public Access policy and resources for researchers to use to comply with this policy Presentations
NCI Central IRB (CIRB) Guidelines PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
NCI CIRB Study Closure Information Formi Word document Form IRB—Institutional Review Board (Human Subject)
NCI CIRB Contact Information Word document Form IRB—Institutional Review Board (Human Subject)
Minor Subjects Only Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Memorandum of Understanding on Academic Exchange PDF document MOU Academic Exchange IIBMST—International Institute of Biomedical Sciences and Technology
Memorandum of Understanding (MOU) between Upstate and Other International Universities PDF document International Institute of Biomedical Sciences and Technology (IIBMST) Memorandum of Understanding IIBMST—International Institute of Biomedical Sciences and Technology
Meeting Dates and Deadlines PDF document Dates and Deadlines IRB—Institutional Review Board (Human Subject)
Meeting Dates and Deadlines PDF document Meeting Dates and Deadlines IBC—Institutional Biosafety Committee
Mandatory Responsible Conduct of Research Education Program PDF document To assure that all Upstate research is performed in a responsible and ethical fashion, all researchers, students, staff, and research personnel musttake a Responsible Conduct of Research course offered by the Collaborative Institutional Training Initiative (CITI) Research Administration
Major Changes to NIH Applications PDF document Information and instructions regarding NIH applications on/after January 25, 2010 Presentations
Investigator Training Program-Research Integrity Part II PDF document Provides information about research misconduct Presentations
Investigator Training Program-Research Integrity Part I PDF document Importance of conflict of interest and the new Upstate Medical University Policy on Relations with the Pharmaceutical, Medical Device & BIotechnology Industry Presentations
Investigator Training Program-Patient Needs Come First PDF document Information about patient needs and safety in clinical research Presentations
Investigator Training Program-Overall Project Management PDF document Managing a clinical trial, including responsibilities of the PI and the project team Presentations
Investigator Training Program-New Initiatives to Promote Clinical Research PDF document Updates regarding Clinical Research Unit, Clinical Trials Office, and availability of inpatient beds for Phase I trials Presentations
Investigator Training Program-Mechanics of Performing a Clinical Trial Part II PDF document Information about pre-award and initial decisions, study start-up, trial progression, and study close out Presentations
Investigator Training Program-Mechanics of Performing a Clinical Trial Part I PDF document Part II of how to conduct a clinical trial at Upstate Medical University Presentations
Investigator Training Program-Considerations for Conducting Studies at Upstate PDF document Information regarding the importance of clinical research and conducting clinical research at Upstate Medical University Presentations
Investigator Self-Assessment Checklisti Word document Self-assessment Checklist QAIP—Quality Assessment & Improvement Program
Investigator Responsibilities for Research Involving a Significant Risk Device PDF document Guidance IRB—Institutional Review Board (Human Subject)
Investigator 101 Education Material PDF document Education Material IRB—Institutional Review Board (Human Subject)
Intramural Research Grant Guidelines PDF document Guidelines for Eligibility and Use of Intramural Research Grant Funds Intramural Research Funding/Grants
Intramural Postdoctoral Fellowship Applicationi Word document Intramural Postdoctoral Research Fellowship Application Form Intramural Research Funding/Grants
Intramural Pilot Grant Applicationi Word document Intramural Research Pilot Grant Application Form Intramural Research Funding/Grants
Intramural Pilot Collaborative Grant Applicationi Word document Intramural Research Pilot Collaborative Research Grant Application Form Intramural Research Funding/Grants
Intramural Bridge Grant Applicationi Word document Intramural Research Bridge Grant Application Form Intramural Research Funding/Grants
Instructions for writing a Biosafety manual PDF document Instructions for writing a Biosafety manual IBC—Institutional Biosafety Committee
Instructions for IRB Protocols Involving Ionizing Radiation Exposure to Human Subjects PDF document Guidelines/Policies RSC—Radiation Safety Committee
Informed Consent Compliance Checklisti Word document Informed Consent Checklist QAIP—Quality Assessment & Improvement Program
Indirect Cost Rate Agreement PDF document Federally negotiated Indirect Cost Rates Research Administration
In Vitro Diagnostocs Decision Tree PDF document Guidance IRB—Institutional Review Board (Human Subject)
IRBNet Training Energizer 2 PDF document IRBNet Training Energizer 2 IRB—Institutional Review Board (Human Subject)
IRBNet Training Energizer 1 PDF document IRBNet Training Energizer 1 IRB—Institutional Review Board (Human Subject)
IRBNet New User Registration and instruction document Word document IRBNet New User Registration and instructions IRB—Institutional Review Board (Human Subject)
IIBMST letter PDF document IIBMST Focus Group Leaders announced IIBMST—International Institute of Biomedical Sciences and Technology
IIBMST Electronic Membership Formi PDF document IIBMST Electronic Membership Form (interactive pdf) IIBMST—International Institute of Biomedical Sciences and Technology
IHP MRI User Request Formi Word document Use this form to request services from the IHP MRI Core Facility Research Facilities
IHP MRI Request Formi PDF document Use this form to request the services of the IHP MRI Core Research Facility Research Facilities
IHP MRI Policy PDF document IHP MRI Core Policy January,2011 update Research Facilities
Human Subjects Research-Unanticipated Problems & Adverse Events PDF document clinical, human subjects research unexpected problems and adverse events Presentations
How to Register for the CITI Basic or Refresher Course PDF document Step by step instructions on registering for the CITI Basic or Refresher Course IRB—Institutional Review Board (Human Subject)
Helpful References PDF document References IBC—Institutional Biosafety Committee
HIPAA and Research PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
HIPAA Review Prepatory to Research Request Form PDF document Form IRB—Institutional Review Board (Human Subject)
HIPAA Required Section Spanish Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
HIPAA Required Section Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Guidelines: Cell Phone Purchases and Monthly Charges on Sponsored Accounts PDF document Guidelines Research Administration
Guidelines for Scientific Reviewers PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Guidelines for Genetic Testing PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Guidance for laboratory workers who work with vaccinia virus (from the CDC) PDF document Vaccinia information IBC—Institutional Biosafety Committee
Guidance for Research Using Lentiviral Vectors PDF document Guidance IBC—Institutional Biosafety Committee
Grant Application Checklist PDF document Checklist of important steps for grant application Research Administration
Genetic Testing: Understanding Definitions and Key concepts PDF document Education IRB—Institutional Review Board (Human Subject)
Genetic Testing & Banking Adults and Children Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Genetic Testing & Banking Adults Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
General Research Policies PDF document An overview of regulatory and contractual policies that govern research and sponsored programs at Upstate and the Research Foundation of the State of New York. General Research Policies
Funding Update March 31-April 4, 2014 PDF document This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information. Funding Update E-mail Alert
Funding Update March 24-28, 2014 PDF document This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information. Funding Update E-mail Alert
Funding Update March 17-21, 2014 PDF document This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information. Funding Update E-mail Alert
Funding Update April 7-11, 2014 PDF document This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information. Funding Update E-mail Alert
Flow Cytometry Fee Schedule PDF document Fee schedule for ust of Flow Cytometry Core Facility updated 2/2/10. Research Administration
Flow Core Fee Schedule PDF document Flow Core Fee Schedule Research Facilities
Finding and Applying for Funding PDF document Information about identifying government and foundation funding and how to apply through Upstate and SU Presentations
Facility Safety Plan PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
FDA Guidance on In Vitro Diagnostics PDF document Guidance IRB—Institutional Review Board (Human Subject)
FDA Guidance on Consent for the use of In Vitro Diagnostics PDF document Guidance IRB—Institutional Review Board (Human Subject)
FCOI Memo from Dr. Goodman PDF document FCOI Memo from Dr. Goodman Research Administration
Exempt Experiments PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
Emergency Use of an Investigational Drug or Biologic PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Emergency Use of Unapproved Medical Devices PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Emergency Use Report Formi Word document Form IRB—Institutional Review Board (Human Subject)
Deans' Grand Rounds 2011 PDF document Grand Rounds Schedule Research Administration
Deans Grand Rounds Wright 2012 PDF document Dr. Wright Research Administration
Data Ownership Policy PDF document Policy describes ownership of data produced at Upstate by faculty, staff, students, fellows, etc. General Research Policies
DHHS Public Health Service Policies on Research Misconduct PDF document Institutions that receive support from Public Health Services offices and agencies, such as NIH, are responsible for following these policies to assure the responsible conduct of research and respond to allegations of research misconduct. General Research Policies
Core Flow Useful Links PDF document Core Flow Useful Links Research Facilities
Core Flow Sort Questionaire PDF document Core Flow Sort Questionaire Research Facilities
Core Flow LSRII PDF document Flow Research Facilities
Core Flow Fortessa Cell Analyzer PDF document Fortessa Cell Analyzer Research Facilities
Core Flow Cell Sorter PDF document Core Flow Cell Sorter Research Facilities
Core Flow Aria Cell Sorter PDF document Core Flow Aria Cell Sorter Research Facilities
Conversations in Entrepreneurship PDF document Conversations in Entrepreneurship Research Administration
Conflict of Interest Policy for IRB Members PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
College Face Sheeti Word document Routing Document for Grant and Clinical Trial application Clinical Trials
Clinical Trials for volunteers PDF document What is a Clinical Trial For Volunteers Clinical Trials
Clinical Trials Registration Policy PDF document Guidelines/Policies Clinical Trials
Clinical Trials Process Flow Sheet PDF document Flow sheet for Sponsored Clinical Trials Clinical Trials
Charge for the Institutional Bio-Safety Committee PDF document Guidelines/Policies IBC—Institutional Biosafety Committee
Case Reports Using Existing Data - Author Worksheeti Word document Case Report Guide IRB—Institutional Review Board (Human Subject)
Carol Baldwin Applicationi Word document Carol Baldwin Grant Application Instructions. Intramural Research Funding/Grants
CTO Fee Schedule Word document Fact Sheet for Institutional fees Clinical Trials
CITI Education Requirement Policy PDF document Mandatory Human Subjects Education Program IRB—Institutional Review Board (Human Subject)
Bosnian Language Standard Consent Sections Word document In Case of Injury, Questions, Voluntary Participation, etc. translated in to Bosnian IRB—Institutional Review Board (Human Subject)
Bosnian Language Signature Pages Word document Signature pages translated into Bosnian IRB—Institutional Review Board (Human Subject)
Bosnian Language HIPAA Section Word document HIPAA section translated into Bosnian IRB—Institutional Review Board (Human Subject)
Biosafety Manual Template for Clinical Research Word document Template IBC—Institutional Biosafety Committee
Biosafety Manual Guidance and Template for Basic Science Research Word document Template IBC—Institutional Biosafety Committee
Biosafety Level 2 Draft Door Sign Word document Door Sign IBC—Institutional Biosafety Committee
Banking Specimens Section Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Assessing Capacity to Consent for Research Word document Form IRB—Institutional Review Board (Human Subject)
Application Form for Recombinant DNA, Bio-hazardous and Infectious Agent Researchi Word document Application Form IBC—Institutional Biosafety Committee
Application Form for Handling, Packaging and Shipping Blood, Tissue or Body Fluids i Word document Application Form IBC—Institutional Biosafety Committee
Amended Informed Consent Regulations (FDA) PDF document Amended informed consent regulations (FDA) IRB—Institutional Review Board (Human Subject)
Adverse Event Guideline PDF document Requirements for notifying the IRB of Unanticipated Events IRB—Institutional Review Board (Human Subject)
Advancing Clinical Research at Upstate-Investigator Training Program PDF document an in-depth course for faculty who conduct human subject research Research Administration
Adult and/or Minor Subjects Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Adult Subjects Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Adult Subjects Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Adult & Minor Subjects Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Additional Study Personnel Form (Appendix A) i Word document Personnel Form IBC—Institutional Biosafety Committee
Access to Patient Information for Research Purposes: Demystifying the Process PDF document Educational Presentation IRB—Institutional Review Board (Human Subject)
2014-2015 Golisano Children's Hospital Research Grant Application Word document Application form to be used to apply for research funding under the Golisano Children's Hospital Program Research Administration
2014-2015 Golisano Children's Hospital Grant Guidelines PDF document Guidelines for applying for research or program funding from the Golisano Children's Hospital Grant Program Research Administration
2014 Summer Student Research/Work Fact Sheet PDF document Provides information to students about summer work and research opportunities Student Research
2014 Summer Student Research Fellowship Application Word document application to be completed by MS1 students in order to be considered for a research fellowship Student Research
"To Whom it May Concern" (Letter for Sponsors Regarding Adverse Events PDF document AE Letter for Spnsors IRB—Institutional Review Board (Human Subject)