- Academic Affairs
- Administration and Finance
- Center for Health and Homeland Security
- Center for Information Technology Services
- Communications and Public Affairs
- Office of Philanthropy
- Government Affairs
- Human Resource Services
- Office of Community Engagement
- Operations and Planning
- Office of the President
- Police and Public Safety
- Research and Development
- University Counsel
The Investigator Manual is designed to guide you through policies, procedures and resources related to the conduct of Human Research that are specific to University of Maryland Baltimore. All human research related activities must be in full compliance with current UMB HRPP and IRB policies and procedures while maintaining compliance with the Federal regulations and assuring the protection of human research participants.
General information regarding Human Research protections and relevant federal regulations and guidance is incorporated into the required human protections training. For additional information, see section: What training do my staff and I need to conduct Human Research?
* All individuals involved in research are expected to be knowledgeable of and follow the guidance outlined in the Investigator Manual
Click To Download a Complete PDF of the Investigator Manual - Version 4-18-2017: Investigator Manual
Click To Review SOPs, Worksheets, and Checklists cited in the Investigator Manual: Referenced Materials
Investigator Manual Online Sections
This document “INVESTIGATOR MANUAL” is designed to guide you through policies, procedures and resources related to the conduct of Human Research that are specific to University of Maryland Baltimore. All human research related activities must be in full compliance with current UMB HRPP and IRB policies and procedures while maintaining compliance with the Federal regulations and assuring the protection of human research participants.
General information regarding Human Research protections and relevant federal regulations and guidance is incorporated into the required human protections training. For additional information, see below: “What training does my staff and I need in order to conduct Human Research?”
Throughout this document “organization” refers to University of Maryland, Baltimore. Please refer to “HRP-001 SOP: Definitions” for additional definitions.
This organization’s Human Research Protection Program (HRPP) is a comprehensive system to ensure the protection of the rights and welfare of participants in Human Research. The Human Research Protection Program is based on all the individuals in this organization along with key individuals and committees fulfilling their roles and responsibilities described in this plan. Please refer to: HRPP Plan
The UMB HRPP maintains a current Federalwide Assurance (FWA Update) (UMB signed Assurance Document) which obligates the Institution to uphold ethical principles and is applicable whenever research is conducted or supported by any U.S. federal department or agency that has adopted the U.S. Federal policy for the Protection of Human Subjects (also known as the Common Rule), unless exempt.
The UMB’s Institutional Review Board (IRB) functions independently, although in coordination with other organizational entities in its role in protecting human research participants. No organizational official or entity at any level can approve research that has not been reviewed and approved by an IRB. Refer to: HRPP Plan
The Human Research Protections Office (HRPO) is the coordinating office for the HRPP and IRB. It is located within the Office of Academic Affairs-Research Compliance and reports to the Institutional Official. Refer to: HRPP Plan
The document HRPP Plan defines the activities that this organization considers to be “Human Research” as defined in DHHS regulations at 45 CFR §46.102(d) and 45 CFR §46.102(f) and as defined in FDA regulations at 21 CFR §56.102(c), 21 CFR §56.102(e), and 21 CFR §812.3(p). An algorithm for determining whether an activity is Human Research can be found in the HRP-309 WORKSHEET - Human Research Determination (Educational Reference Only). Use this document for guidance as to whether an activity meets either the DHHS or FDA definition of Human Research, keeping in mind that the IRB makes the ultimate determination in questionable cases as to whether an activity constitutes Human Research subject to IRB oversight. You are responsible not to conduct Human Research without prior IRB review and approval (or an IRB determination that the Human Research is Exempt). If you have questions about whether an activity is Human Research, request a determination from the Human Research Protections Office (HRPO) via CICERO. See below “How do I submit new Human Research to the IRB?” Also, see below “What are the different regulatory classifications that research activities may fall under?”
The document HRPP Plan describes this organization's overall plan to protect participants in Human Research:
- The mission of the Human Research Protection Program.
- The ethical principles that the organization follows governing the conduct of Human Research.
- The applicable laws that govern Human Research.
- When the organization becomes "engaged in Human Research" and when someone is acting as an agent of the organization conducting Human Research.
- The types of Human Research that may not be conducted.
- The roles and responsibilities of individuals within the organization
You are considered “engaged” in human participants’ research when you
1) intervene or interact with living individuals for research purposes, or
2) obtain individually identifiable private information for research purposes.
Further, a site is considered to be “engaged” in human participants’ research when it receives a direct Federal award to support the research.
See: HRP-310 - WORKSHEET - Engagement Determination
To qualify as a principal investigator, you must be a full-time (>51% effort) faculty member holding one of the following titles at UMB:
- Associate Professor
- Assistant Professor
If you do not hold one of the above positions and wish to become a principal investigator, you must submit a written request with justification and your curriculum vitae for consideration by the Institutional Official. Contact:
Name: Julie Doherty, RN, MSN
Title: Director, Human Protections Administrator
620 W. Lexington Street, Second Floor
Baltimore, Maryland 21201
Phone: (410) 706-3867
This request must also include a written agreement from a faculty member who meets the requirements of a principal investigator to mentor you on the conduct of human subject research. Students and fellows are not permitted to be Principal Investigators.
The IRB recognizes one Principal Investigator for each project. The Principal Investigator bears the ultimate responsibility for assuring that the conduct of the study complies with all UMB HRPP policies and procedures for the protection of human participants.
When the Principal Investigator for clinical studies involving medical/clinical interventions or investigational agents does not have a medical degree (M.D.), there must be at least one sub-investigator on the project that is a qualified M.D. with the appropriate expertise for the study.
All individuals involved in the design, conduct and/or reporting of research must be adequately qualified and licensed relevant to the scope and complexity of the research conducted and their role in the research.
All individuals involved in the design, conduct and/or reporting of research must be familiar with and know how to apply the ethical principles of The Belmont Report, current Federal and State laws and regulations, current institutional policies and procedures, and Good Clinical Practice standards (See Appendix A ) when conducting research involving humans at UMB.
All individuals involved in the design, conduct and/or reporting of research must complete the online Collaborative Institutional Training Initiative (CITI) human participants online training program as well as HIPAA training. IRB approval will not be granted for proposed research in which the principal investigator has not completed the required human research protections training and HIPAA training listed below. The principal investigator of each research project is responsible for ensuring that all individuals involved in the design, conduct and/or reporting of the research have also completed the required training.
The CITI site can be accessed at www.citiprogram.org. This training is valid for a three year period, after which time a refresher CITI course must be completed. A minimum score of 80% overall must be obtained for CITI training.
All UMB employees are required to complete HIPAA 125 training. In addition, individuals involved in the design, conduct and/or reporting of research are required to complete HIPAA 201 training. Both of these trainings can be accessed at http://somvweb.som.umaryland.edu/hipaa/quiz/index.asp.
Individuals that are external to the UMB system and are involved in the design, conduct and/or reporting of research conducted at UMB must have completed their employer’s required certifications or trainings. External Investigators must supply their CV and proof of the required certifications or trainings to the UMB Principal Investigator under which they are working. The UMB Principal Investigator will be responsible for forwarding these to the HRPO Office when requested.
- Make sure that you have the adequate resources to protect the rights, welfare and safety of human participants involved in the research, including:
- Sufficient time to conduct, oversee and complete research
- Adequate number of qualified staff
- A process to ensure that all persons involved in the design, conduct and/or reporting of research are adequately informed about the protocol and their research-related duties and functions
- Adequate facilities in which to perform study procedures
- Availability of medical or psychological resources that participants may need as a consequence of the research
- Access to a population that will allow recruitment of the necessary number of participants.
- Make sure that the research application is consistent with the proposal for funding for extramural or intramural support
- Act as a liaison between the IRB and the research sponsor (e.g., notification of IRB review and approval).
- Make sure that there are additional protections for research involving vulnerable populations as required.
- If your research involves entities within UMB that are not under your control, you must ensure appropriate communication, education, and training of those staff.
- Refer to the Center for Clinical Trials and Corporate Contracts (CCT) website for information regarding correct research billing procedures: Clinical Trials and Corporate Contracts
- If your research is sponsored by a commercial sponsor, please refer to the Corporate Contracts section of the CCT website: Clinical Trials and Corporate Contracts
- If your research is sponsored by a federal agency, foundation or other non-profit organization, please see Sponsored Program Administration section on the Research @ UMB website: Sponsored Programs Administration
- If your research involves investigational drugs, biologics, or devices, you must follow HRP-092 SOP: Control of Investigational Test Articles.
Your research may be regulated by more than one federal agency, depending on the project funding and type of project. Regardless of funding source, all human participant research must meet the regulatory criteria for approval. See HRP-311 - WORKSHEET - Criteria for Approval and Additional Considerations.
- If your research is funded by a federal agency, you are required to follow Department of Health and Human Services (DHHS) regulations at 45 CFR 46. Also refer to Appendix A for more information.
- If your research involves drugs or devices, you are required to follow Food and Drug Administration (FDA) regulations at 21 CFR 50 and 21 CFR 56. Also refer to Appendix A for more information.
- If your research involves the use of a drug with an active Investigational New Drug (IND) application, you are required to follow FDA regulations at 21 CFR 312. Also refer to Appendix A for more information.
- If you are the IND holder, you are required to follow both the Investigator responsibilities and Sponsor responsibilities at 21 CFR 11, 21 CFR 54, 21 CFR 210, 21 CFR 312, 21 CFR 314, 21 CFR 320, 21 CFR 330, and 21 CFR 601.
- If your research involves the use of a device with an active Investigational Device Exception (IDE), you are required to follow FDA regulations at 21 CFR 812. Also refer to Appendix A for more information.
- If you are the IDE holder, you are required to follow both the Investigator responsibilities and Sponsor responsibilities at 21 CFR 11, 21 CFR 54, 21 CFR 812, 21 CFR 814, 21 CFR 820, and 21 CFR 860.
- If your research involves the use of veterans, Veterans Health Administration (VHA) funding or other VA resources, you are required to follow regulations in VHA Handbook 1200.05. Also refer to Appendix A for more information.
- If your research involves funding by a federal agency other than DHHS and NIH, you are required to follow regulations pertaining to those agencies:
- Department of Defense – see Appendix A
- Department of Energy – see Appendix A
- Department of Education – see Appendix A
Yes, the IRB charges to review certain research proposals for Industry-Supported Applications.
Contact the Center for Clinical Trails and Corporate Contracts office for further information.
Complete a CICERO application, attach all required documents and submit to the HRPO. If you are unsure if the project is human participants research, refer to HRP-309 WORKSHEET - Human Research Determination (Educational Reference Only)
** All research proposals require a CICERO application.
- Abbreviated Title: Enter the abbreviated title. This is the title that will appear in the CICERO application
- Full Title: Enter the full protocol name. This title will be entered into the determination letter.
- Select Type of Submission: Select the appropriate type of su
- Application: Select whether or not you have an existing research protocol. This can be a sponsor’s protocol or other type of protocol that has all of the required information. See below “How do I write an Investigator Protocol?”
Complete the remaining sections in the application as appropriate. Remember that if you have an existing protocol, you can reference sections or page numbers of that protocol in the CICERO application. Read all of the instructions for each section. Provide all the information requested, as appropriate for the research protocol.
- Principal Investigator – Name the person with overall responsibility for the conduct of the Human Research. There can only be one investigator with this overall responsibility. If you are not listed on the Principal Investigator dropdown list, see above section “Can I be a principal investigator for a study?” to determine if you meet the criteria for Principal Investigator privileges. If you meet the criteria, please contact HRPO at 410-706-5037 or firstname.lastname@example.org for assistance.
- Point of Contact – Who is the alternative point of contact for the Principal Investigator. This person can be a study coordinator or any other study team member. In case the IRB cannot contact the Principal Investigator, this person is a secondary person to contact. A person listed as Point of Contact (POC) cannot also be listed under “Other Team Members.”
- Other Team Members – List all Human Research personnel involved in the design, conduct, or reporting of the Human Research and their roles. This includes all co-investigators, sub-investigators, coordinators, assistants, students, and collaborators who have a role in the design, conduct, or reporting of the Human Research.
When adding each person, you must select whether or not to give “edit rights.” Selecting “yes” will allow the person to edit the online forms and to execute activities (protocol modifications, reportable events, etc) in CICERO. Note: granting a person edit rights will automatically add them to the email CC list and this person will receive all emails from CICERO to the team regarding the submission. In addition, for each person added, you must select whether or not they will receive emails sent to the Principal Investigator by CICERO and the HRPO.
Each person who is added to the protocol must complete a Conflict of Interest statement. CICERO will send each person an email. Individuals must update their Conflict of Interest statement within 10 days of the becoming aware of any change in a financial interest that affects this statement. The principal investigator is responsible for ensuring that all investigators and research staff comply with this requirement. When there are questions about the qualifications of research team members, the Organizational Official can be consulted and make determinations about further actions.
Approvals Required Prior to Initiating Research
Check all additional approvals that are required:
- Radiation being used for reasons other than clinical care
- The use of any biohazards
- Research involving human gene transfer or immune response
- Research involving cancer
- Research using VA patients, facilities or personnel
Department Scientific and Feasibility Review
All new research submissions must undergo Department Scientific and Feasibility Review. If your research involves a department other than your department, a specialty review must also be completed. For example, your research involves children (review required from the Department of Pediatrics) or cancer (review required from the Greenebaum Cancer Center). CICERO will send reviews to these departments automatically when you submit the application. When the Department Chair is the principal investigator (PI), the Department Scientific and Feasibility Review must be completed by an individual outside of the PI's department.
All research submissions must either have a completed application form in CICERO or a separate research protocol attached and referenced in CICERO. Follow the application instructions in CICERO. If you have a sponsor’s protocol, you may reference pages in the sponsor’s protocol in the corresponding sections of the CICERO application. Here are some key points to remember when completing the CICERO application or creating your own separate research protocol document:
- For an Investigator Protocol document:
- the italicized bullet points in the templates serve as a guide to investigators when developing an Investigator Protocol for submission to the IRB. All italicized comments are meant to be deleted prior to submission.
- Note that, depending on the nature of your research, certain sections of the template may not be applicable to your Investigator Protocol. Skip these sections as appropriate.
- You may not involve any individuals who are members of the following populations as participants in your research unless you indicate this in your inclusion criteria as the inclusion of participants in these populations requires additional protections. Students and employees may be enrolled like any other vulnerable population. CICERO will provide additional information and requirements for these vulnerable populations:
- Adults unable to consent
- Individuals who are not yet adults (infants, children, teenagers)
- Pregnant women
Use the Consent Form Templates to create a consent document. Note that all consent documents must contain all of the required and all additional appropriate elements of informed consent disclosure. Review section 7 of the HRP-311 - WORKSHEET - Criteria for Approval and Additional Considerations to ensure that these elements are addressed. For research involving the VA, you must use a VA consent form, VA 10- 1086.
Note that all long form consent documents and all summaries for short form consent documents must contain all of the required and all additional appropriate elements of informed consent disclosure. Review the “Long Form of Consent Documentation” section in the IRB’s HRP-311 - WORKSHEET - Criteria for Approval and Additional Considerations to ensure that these elements are addressed. When using the short form of consent documentation, the appropriate signature block from “TEMPLATE CONSENT DOCUMENT” should be used on the short form.
We recommend that you date the revisions of your consent documents in the footer section to ensure that you use the most recent version approved by the IRB.
Participants who do not speak English should be presented with informed consent documents in a language understandable to them that includes all the required and additional elements for disclosure. Either the long form of the consent document needs to be translated in writing into the subject’s language or the short form of consent document may be used. With the short form of consent documentation, the long form of consent may be translated orally and only a small portion of the information translated into the subject’s language.
Please see below “How do I document consent?” and the requirement for the short form consent on HRP-318 - WORKSHEET - Short Form of Consent Documentation.
Ensuring Appropriate Telephone Contact with Subjects. This pertains to contacting the subject by telephone. Research team members are prohibited from requesting Social Security numbers by telephone.
- Initial Contact. During the recruitment process, ensuring the research team makes initial contact with the potential subject in person or by letter prior to initiating any telephone contact, unless there is written documentation that the subject is willing to be contacted by telephone about the study in question or a specific kind of research (e.g., if the potential subject has diabetes, the subject may indicate a desire to be notified of any diabetes-related research studies) or the IRB has determined otherwise, with appropriate justification. NOTE: One source of information about clinical trials that can be shared with potential subjects is the NIH clinical trials Web site (http://www.clinicaltrials.gov) where clinical trials are listed.
- Later Contact. Ensuring the research team begins telephone calls to the subject by referring to previous contacts and, when applicable, the information provided in the informed consent form, and ensuring that the scope of telephone contacts with the subject is limited to topics outlined in IRBapproved protocols and informed consent forms.
The IRB may approve a consent procedure which does not include, or which alters, some or all of the required elements of informed consent. Refer to HRP-415 - CICERO CHECKLIST - Waiver or Alteration of the Consent Process. Also, the IRB may approve a consent procedure which waives the requirements to obtain written informed consent entirely. Refer to HRP-416 - CICERO CHECKLIST - Waiver of Written Documentation of the Consent Proc.
The Health Insurance Portability and Accountability Act (HIPAA) regulates how protected health information can be used and disclosed. An investigator must obtain an authorization via a HIPAA Authorization Form from all participants in research prior to the use or disclosure of protected health information (PHI) for any research related purpose. PHI is any information in the medical record or designated record set that can be used to identify an individual. In addition, refer to HRP-331 - WORKSHEET - HIPAA Authorizations for Research for elements required in a HIPAA Authorization Form.
The IRB can waive or alter the requirement for HIPAA Authorization for study recruitment purposes or for the entire study. Refer to HRP-441 - CICERO CHECKLIST - HIPAA Waiver of Authorization
Certain research projects are required to register at the website ClinicalTrials.gov. These projects are also responsible to update records and report results per policy. Refer to: “HRP-095 - SOP Clinical Trials” and “ClinicalTrials.gov Instructions for the Research Community”.
Submitted activities may fall under one of the following four regulatory classifications:
- Not “Human Research”: Activities must meet the DHHS or FDA definition of “research” involving “human participants” for the activity to fall under IRB oversight. Activities that meet neither definition of “Research” involving “Human Participants” are not subject to IRB oversight or review. Refer to HRP-309 WORKSHEET - Human Research Determination (Educational Reference Only). Contact the Human Research Protections Office (HRPO) in cases where it is unclear whether an activity meets the regulatory definition of Human Research.When a project is determined to be nonhuman subject research, that determination is made by the particular information provided in the CICERO application. If you make any changes to the project, you must submit a protocol modification to determine if the project remains nonhuman participant research.
- Exempt: Certain categories of Human Research may be exempt from regulation but require IRB review. It is the responsibility of the IRB, not the investigator, to determine whether Human Research is exempt from IRB review. Refer to HRP-401 - CICERO CHECKLIST - Pre-Review and Administrative Review for reference on the categories of research that may be exempt. When a research study is determined to be exempt, that determination is made on the particular information provided in the CICERO application. If you make any changes to an exempt study, you must submit a protocol modification to determine if the research study continues to meet the exemption status.
- Review Using the Expedited Procedure: Certain categories of non-exempt Human Research may qualify for review using the expedited procedure. Refer to HRP-401 - CICERO CHECKLIST - Pre-Review and Administrative Review for reference on the categories of research that may be reviewed using the expedited procedure.
- Review by the Convened IRB: Non-Exempt Human Research that does not qualify for review using the expedited procedure must be reviewed by the convened IRB.
The IRB may approve research, require modifications to the research to secure approval, table research, defer research or disapprove research:
- Approval: Made when all criteria for approval are met. See “How does the IRB decide whether to approve Human Research?” below.
- Modifications Required to Secure Approval: Made when the IRB requires specific modifications to the research before approval can be finalized. See section below “What will happen after IRB review?”
- Deferred: Made when the IRB determines that it is unable to approve research and the IRB has recommendations that might make the protocol approvable. When this motion is made, the IRB describes its reasons and recommendations. See section below “What will happen after IRB review?”
- Disapproval: Made when the IRB determines that it is unable to approve research and the IRB cannot describe modifications that might make the research approvable. When this motion is made, the IRB describes its reasons. See section below “What will happen after IRB review?”
- Tabled: Made when the IRB cannot approve the research at a meeting for reasons unrelated to the research, such as loss of quorum. These are often administrative reasons. When taking this action, the IRB automatically schedules the research for review at a future meeting.
The criteria for IRB approval can be found in HRP-311 - WORKSHEET - Criteria for Approval and Additional Considerations for non-exempt Human Research. The latter worksheet references other checklists that might be relevant. All checklists and worksheets can be found on the HRPO Web site.
These checklists and worksheets are used for initial review, continuing review, and review of modifications to previously approved Human Research.
YOU ARE ENCOURAGED TO USE THE CHECKLISTS AND WORKSHEETS TO WRITE YOUR INVESTIGATOR PROTOCOL IN A WAY THAT ADDRESSES THE CRITERIA FOR APPROVAL.
The IRB will provide you with a written determination indicating that the IRB has approved the Human Research, requires modifications to secure approval, or has deferred, tabled, or disapproved the Human Research.
The IRB can approve a research project for no more than 365 days. The Federal regulations make no provision for any grace period extending the conduct of research beyond the expiration date of IRB approval; therefore, continuing review and re-approval of research must occur before the date when IRB approval expires. If this does not happen, all research activities must cease. See section below “What do I do if my study expires?”
- If the IRB has approved the Human Research: The Human Research may commence once all other organizational approvals have been met. IRB approval is good for a limited period of time, which is noted in the approval letter.
- If the IRB requires modifications to secure approval and you accept the modifications: Make the requested modifications and submit them to the IRB as soon as possible via CICERO. If all requested modifications are made, the IRB will issue a final approval. Research cannot commence until this final approval is received. If you do not respond to the IRB within 30 days, the offer of approval with the requested modifications will be withdrawn. If you do not accept the modifications, write up your response and submit it to the IRB within 30 days. If you do not provided additional information or correspondence within 30 days, and the IRB will require a complete new submission.
- If the IRB defers the Human Research: The IRB will provide a statement of the reasons for deferral and any recommendations that might make the protocol approvable. Make the recommended changes and respond to each of the IRB’s questions/concerns and submit them to the IRB as soon as possible via CICERO. Once a complete response has been received, the submission will be scheduled for review at an IRB meeting.
- If the IRB disapproves the Human Research: The IRB will provide a statement of the reasons for disapproval. If the investigator wishes to pursue the research project, a new CICERO application must be submitted.
In all cases, you have the right to address your concerns to the IRB directly at an IRB meeting. To request this, contact the Director, Regulatory Compliance.. You may address the IRB panel via teleconference.
Depending on the type of research you do, where it is done, what procedures are involved and other factors, your research proposal may need to be reviewed by a committee in addition to the IRB. Some of these required approvals will be captured by your CICERO application.
For VA research the investigators must submit the appropriate documentation to the VA R&D Committee for initial review and approval. Investigators must also submit modification documentation to the VA R&D committee for review and approval for any modifications related to biosafety or radiation safety.
- Do not start Human Research activities until you have the final IRB approval letter (including washout and screening).
- Do not start Human Research activities until you have the approval of departments or divisions that require approval prior to commencing research that involves their resources. CICERO will automatically send notification to the required departments from the questions you answer within your CICERO application. You will be able to see the department’s responses in CICERO’s history log for your study.
- Do not start Human Research activities until organizational approvals are met. See "Approvals Required Prior to Initiating Research".
- Personally conduct or supervise the Human Research.
- Protect the rights, safety, and welfare of participants involved in the research.
- Conduct the Human Research in accordance with the relevant current protocol as approved by the IRB, and in accordance with applicable federal regulations and local laws.
- Assure that each participant is adequately informed and freely consents to participate in the research, unless a waiver of consent has been obtained from the UMB IRB. The Principal Investigator must personally assure that every reasonable precaution is taken to reduce risks to participants.
- Delegate responsibility to the research staff in accordance with the staff’s training and qualifications.
- Assure that all procedures associated with the research are performed, with the appropriate level of supervision, only by individuals who are licensed or otherwise qualified to perform them under the laws of Maryland and polices of the University of Maryland, Baltimore.
- Monitor the research study and perform quality management activities to ensure the protection of participants and the quality of the research data. Deficiencies identified during quality improvement processes must be addressed in a timely manner. Refer to “CHECKLIST: Investigator Quality Improvement Assessment” for more information.
- Do not modify the Human Research without prior IRB review and approval unless necessary to eliminate apparent immediate hazards to participants.
- Changes in approved research that are initiated without IRB approval to eliminate apparent immediate hazards to the participant are promptly (within 5 days) reported to the IRB and are reviewed by the IRB to determine whether each change was consistent with ensuring the participants’ continued welfare.
Changes in approved research that are initiated without IRB approval to eliminate apparent immediate hazards to the participant are promptly (within 5 days) reported to the IRB and are reviewed by the IRB to determine whether each change was consistent with ensuring the participants’ continued welfare.
- Submit to the IRB:
- Proposed modifications as described in this manual. See below “How do I submit a modification?”
- A continuing review application no later than 6 WEEKS PRIOR to the expiration date found in the IRB approval letter for your study. See below “How do I submit a continuing review?”
- A closure report when the Human Research is closed. See below “How Do I Close Out a Study?”
- Do not accept or provide payments to professionals in exchange for referrals of potential participants (“finder’s fees.”)
- Do not accept payments designed to accelerate recruitment that were tied to the rate or timing of enrollment (“bonus payments.”)
- Be open to participants’ complaints or requests for information. Investigators and research staff should follow a process to respond appropriately to such complaints.
- Notify the IRB of any participant or other individual’s complaints regarding the research. The complaint may be reported at continuing review if it involves no risk to the participants or others or does not change the risk/benefit analysis (e.g., a participant complains that he/she does not like the investigator’s clinic hours and subsequently withdraws from the research).
- Report complaints that involve potential risks to participants or others or result in a possible change in the risk/benefit analysis as an unanticipated problem as soon as possible, but no later than FIVE WORKING DAYS after the investigator first learns of the complaint (e.g., a member of the research team where the research is conducted complains that the research assistant has not maintained her research notes in a confidential manner which may have potentially breached confidentiality).
- See additional requirements of various federal agencies in Appendix A.
Consent to participation in research is documented by the use of an informed consent document that has been signed by the participant or the participant’s legally authorized representative. Use the signature block approved by the IRB. Complete all items in the signature block. Refer to HRP-090 SOP: Informed Consent Process for Research and HRP-091 SOP: Written Documentation of Consent
The following are the requirements for long form consent documents:
- The subject or representative signs and dates the consent document.
- The individual obtaining consent signs and dates the consent document.
- Whenever required by the IRB the subject’s or representative’s signature is to be witnessed by an individual who signs and dates the consent document.
- For participants who cannot read and whenever required by the IRB or the sponsor, a witness to the oral presentation signs and dates the consent document.
- A copy of the signed and dated consent document is to be provided to the subject.
- For Veterans Administration (VA) research, consent must be documented on a Veterans Administration (VA) Form 10-1086.
The following are the requirements for short form consent documents:
- The subject or representative signs and dates the consent document.
- The individual obtaining consent signs and dates the summary.
- The witness to the oral presentation signs and dates the consent document and the summary. The person obtaining consent may not be the witness to the consent.
- A copy of the signed and dated consent document and a copy of the signed and dated summary are to be provided to the person signing the document.
- For Veterans Administration (VA) research, consent must be documented on a Veterans Administration (VA) Form 10-1086.
Certain information must be reported to the IRB in a prompt manner, within FIVE (5) business days of the investigator becoming aware of the information. See Study Conduct section “REPORTABLE NEW INFORMATION BULLETIN” for a list of information that is requires prompt reporting.
All other events can be reported to the IRB in an aggregate fashion at the time of continuing review.
Complete the “Create Modification” application in CICERO. Attach relevant documents and submit. Please note that research must continue to be conducted without inclusion of the modification until IRB approval is received.
The IRB must determine if any criteria for approval are affected by the modification and if so, that the particular criterion continues to be met. See HRP-311 - WORKSHEET - Criteria for Approval and Additional Considerations For additional information, refer to HRP-021 SOP: Pre-review and HRP-401 - CICERO CHECKLIST - Pre-Review and Administrative Review.
Complete the “Create Continuing Review” application in CICERO. Attach relevant documents including any data safety monitoring committee review, and submit. A Continuing Review application must be submitted at least 6 WEEKS PRIOR TO THE EXPIRATION DATE of the IRB approval indicated in the approval letter.
During continuing review the IRB must determine if the criteria for approval continues to be met. See HRP-311 - WORKSHEET - Criteria for Approval and Additional Considerations For additional information, refer to HRP-021 SOP: Pre-review and HRP-401 - CICERO CHECKLIST - Pre-Review and Administrative Review.
If the IRB approval for your study expires, all Human Research procedures related to the protocol under review must cease, including recruitment, advertisement, screening, enrollment, consenting, interventions, interactions, and collection of research data. In addition, any data analyses of previously collected research data must cease. Continuing Human Research procedures without IRB approval is a violation of federal regulations.
If current participants will be harmed by stopping human research procedures that are available outside the human research context, provide these on a clinical basis as needed to protect current participants. If current participants will be harmed by stopping human research procedures that are not available outside the human research context, immediately contact the IRB chair for guidance. Remember that research data cannot be collected during study expiration.
To be eligible for closure, the IRB study must meet all of the following criteria:
- Data collection is complete;
- There is no more participant contact, including phone calls, long term follow up, data collection visits, and surveys;
- The only research activity being conducted is data analysis of de-identified data.
Complete the “Closure Report” in CICERO. Attach relevant documents and submit the report. A Closure Report must be submitted within 45 days of study closure. If you fail to submit a Closure Report to close out Human Research, you will be restricted from submitting new Human Research until the completed application has been received.
If the Closure Report for closing out a Human Research study is not received by the date requested in the approval letter, you will be restricted from submitting new Human Research until the completed application is received.
If your IRB approval lapses for any reason, your new research applications will not be reviewed by the IRB. Also, if you fail to submit a protocol continuing review by the date requested on the approval letter or you fail to submit a protocol closure report within 45 days of the end of the study, your new research applications will not be reviewed by the IRB. You will know you are on the restricted list if your name appears in red on any of your research protocols in CICERO.
Once you have submitted the outstanding continuing review or protocol closure report, your name will be taken off the restricted list.
Maintain your Human Research records, including signed and dated consent documents for at least THREE YEARS after completion of the research. Maintain signed and dated HIPAA authorizations and consent documents that include HIPAA authorizations for at least SIX YEARS after completion of the research.
If your Human Research is sponsored, contact the sponsor before disposing of Human Research records.
If your research is regulated by the FDA, refer to Appendix A for specific research record retention guidelines.
If your research involves the VA, refer to Appendix A for specific research record retention guidelines.
If you are planning to move to another location and leave UMB, the IRB must be notified. You can either have another UMB investigator assume Principal Investigator responsibilities, or you can close each of your research studies with the IRB, or you can transfer the research studies to the new location.
You must also notify the IRB in writing of the plan for either destroying the data or transferring the data to another Principal Investigator. The original research study documents are the property of UMB and must remain at UMB.
Contact the Human Research Protections Office (HRPO) or IRB chair immediately to discuss the situation. If there is no time to make this contact, see the HRP-317 - WORKSHEET - Emergency Use of a Test Article for the regulatory criteria allowing such a use and make sure these criteria are followed. You will need to submit a report of the use to the IRB WITHIN FIVE DAYS of the use and an IRB application for initial review WITHIN 30 DAYS.
If you fail to submit the report within five days or the IRB application for initial review within 30 days, you will be restricted from submitting new Human Research until the report and IRB application for initial review have been received. For additional information, see HRP-023 SOP: Emergency Use of a Test Article Review.
Emergency use of an unapproved drug or biologic in a life-threatening situation without prior IRB review is “research” as defined by FDA, the individual getting the test article is a “subject” as defined by FDA, and therefore is governed by FDA regulations for IRB review and informed consent. Emergency use of an unapproved device in a lifethreatening situation without prior IRB review is not “research” as defined by FDA and the individual getting the test article is not a “subject” as defined by FDA. However, FDA guidance recommends following similar rules as for emergency use of an unapproved drug or biologic.
Individuals getting an unapproved drug or device in a life-threatening situation without prior IRB review cannot be considered a “subject” as defined by DHHS and their results cannot be included in prospective “research” as that term is defined by DHHS.
Please see HRP-415 - CICERO CHECKLIST - Waiver or Alteration of the Consent Process for the criteria that IRB needs to determine are met to approve the conduct of such research.
This document and the policies and procedures for the Human Research Protection Program are available on the HRP website.
If you have any questions or concerns, about the Human Research Protection Program, contact the Human Research Protections Office (HRPO) at:
Human Research Protections Office
620 W. Lexington Street, Second Floor
Baltimore, Maryland 21201
If you have questions, concerns, complaints, allegations of undue influence, allegations or findings of non-compliance, or input regarding the Human Research Protection Program that cannot be addressed by contacting the Human Research Protections Office (HRPO), follow the directions in the “HUMAN RESEARCH PROTECTION PROGRAM PLAN” under “Reporting and Management of Concerns.”
Appendix A-1 - Additional Requirements for DHHS-Regulated Research
Appendix A-2 - Additional Requirements for FDA-Regulated Research
Appendix A-3 - Additional Requirements for Clinical Trials (ICHGCP)
Appendix A-4 - Additional Requirements for Department of Defense (DOD) Research
Appendix A-4 - Additional Requirements for Department of Navy (DON) Research
Appendix A-5 - Additional Requirements for Department of Energy (DOE) Research
Appendix A-6 - Additional Requirements for Department of Education (ED) Research
Appendix A-7 - Additional Requirements for Veterans Administration (VA) Research
Appendix A-8 - Additional Requirements for Department of Justice (DOJ) Research
Appendix A-8 - Additional Requirements for the Department of Justice (DOJ) Research Funded by the National Institute of Justice