U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

Similar documents
U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

Specialty Y/N. Internal Medicine Y PS-Physician Scientist; Vice-Chair. Alternative Members

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

This policy defines the composition and requirements of the North Shore Medical Center (NSMC) Institutional Review Board (IRB) membership.

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

IRB MEMBERSHIP COMPOSITION, ROLES AND RESPONSIBILIES

IRB COMPOSITION AND IRB MEMBER ROLES AND RESPONSIBILITIES

U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB)

SOP Institutional Review Board (IRB) Appointments and Membership

CONTINUING REVIEW 3/7/2016

To assure knowledge and compliance by documenting the annual administrative review and continuing IRB review of non-exempt projects for the IRB.

2.0 Institutional Review Board

Oklahoma State University Institutional Review Board Standard Operating Procedures

UNIVERSITY OF TENNESSEE GRADUATE SCHOOL OF MEDICINE INSTITUTIONAL REVIEW BOARD CONTINUING REVIEW AND REAPPROVAL OF RESEARCH

Category Description This policy and procedure applies to the Sparrow research community.

Human Research Protections Program Medical College of Wisconsin and Froedtert Memorial Lutheran Hospital

Issue in IRB Approvals:

To assure knowledge and compliance by documenting the continuing review procedure of approved projects for the IRB.

USC Institutional Review Boards (IRBs)

SOP 5.06 Full Committee Review: Initial IRB Review

2 Institutional Review Board

Wayne State University Institutional Review Board

Institutional Responsibilities Under A Federalwide Assurance

CONTINUING REVIEW OF APPROVED IRB PROTOCOLS

UNIVERSITY OF TENNESSEE GRADUATE SCHOOL OF MEDICINE INSTITUTIONAL REVIEW BOARD PROCEDURES FOR FULL BOARD REVIEW

UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER INSTITUTIONAL REVIEW BOARD CONTINUING REVIEW OF RESEARCH

OHRP Guidance on Written IRB Procedures

Review of Research by the Convened IRB

Research and IRB Review FAQs

Independent Ethics Committees

What s New in GCP? FDA, OHRP Issue Harmonized Guidance on Transferring IRB Oversight of Clinical Studies

NONCOMPLIANCE. 1. Overview

IV. Basic Procedures for Human Research Protections

Investigator Manual. If you have questions about whether an activity requires IRB review, contact the IRB Office.

IRB Chair Responsibilities

Research Involving Human Subjects: AA 110.7

Effective Date Revisions Date Review by the Convened Institutional Review Board

JUN L WARNING LETTER VIA FEDERAL EXPRESS

CONTINUING REVIEW CRITERIA FOR RENEWAL

Effective Date: January 16, 2012 Policy Number: MHC_RP0107. Revised Date: November 2, 2015 Oversight Level: Corporate

Institutional Review Board Submission Requirement Presentation

IRB Minutes Quality Improvement Assessment

I. Summary. II. Responsibilities

Harford Community College. Institutional Review Board Charter and Standard Operating Procedures

UNIVERSITY OF GEORGIA Institutional Review Board

Yale University Human Research Protection Program

MISSISSIPPI STATE UNIVERSITY HUMAN RESEARCH PROTECTION PROGRAM. Collaborative Research and Performance Sites (01-23) Approved

SOP 801: Investigator Qualifications and Responsibilities

INSTITUTIONAL REVIEW BOARD (IRB) PROCEDURES

Guidance for IRBs, Clinical Investigators, and Sponsors IRB Continuing Review after Clinical Investigation Approval

Institutional Review Board - Restriction s Impo sed

Institutional Review Board Standard Operating Procedure. Suspension and Termination of IRB Approval

University of Pennsylvania Institutional Review Board. Reliance Agreement Guidance: Penn as Central IRB FAQ

University of Cincinnati. Radiation Safety Committee Operations Guidelines Statement of Policy (RSC Guidelines) RSC Guidelines (revision 5)

Children s Hospital of Philadelphia Committees for the Protection of Human Subjects Policies and Procedures. IRB Review Processes

Submitting Continuing Reviews and/or Amendments to the IRB

CONTINUING REVIEW CRITERIA FOR RENEWAL

INSTITUTIONAL REVIEW BOARD (IRB) PROCEDURES

Reporting an Unanticipated Problem Involving Risks to Subjects or Others (UPIRTSO) to the IRB

(y9. &i?r, JUL t Certified-Return Receipt Requested WARNING LE7TER

Policies & Standard Operating Procedures

University of Kentucky Office of Research Integrity and Institutional Review Board Standard Operating Procedures SOP #4-1 Revision #6

INSTITUTIONAL REVIEW BOARD MANUAL: PURPOSE and POLICIES.

Institutional Review Board Policies and Procedures

Procedure Department: HUMAN RESEARCH PROTECTIONS PROGRAM Policy Number: II.B.1

GUIDE TO DAILY OPERATIONS

Lapse in IRB Approval

Yale University Institutional Review Boards

OTM Patent Coordinator. Biomedical and Health Information Sciences Lauren Segal Anne Burkhart Architecture, School of Mark Krivchenia Anne Burkhart

Food and Drug Administration Center for Devices an d * 1Ya I a Radiological Health WARNING LETTE R

Standard Operating Policy and Procedures (SOPP) 3:

Michigan State University Human Research Protection Program

Institutional Review Board (IRB) Policies and Procedures Manual

INSTITUTIONAL REVIEW BOARD PROCEDURES

Initial Review. Approved By: Michele Kennett, JD, MSN, LLM Associate Vice Chancellor for Research. Table of Contents

EMERGENCY USE 03/02/2016

Ceded IRB Review. The University of Arizona has standing agreements in place for the following entities regarding ceded IRB review:

Children s Hospital of Philadelphia Committees for the Protection of Human Subjects Policies and Procedures Continuing Review of Approved Research

Human Research Protection Program. Institutional Review Board

SYRACUSE UNIVERSITY HUMAN RESEARCH PROTECTION PROGRAM STANDARD OPERATING PROCEDURES

Info Sheet - Operations Office for Human Research Studies

SUSPENSION OR TERMINATION OF HUMAN SUBJECTS RESEARCH

SOP #2-2 Version #1 Date First Effective: December 14, Page 1 of 6

Arkansas Tech University Institutional Review Board

The Top 10 Human Research Protection Compliance Risks

CUNY HRPP Procedures: Multisite Non-Exempt Human Subjects Research

University of Pennsylvania Institutional Review Board. Reliance Agreement Guidance: How to Apply for External IRB Review

Office of the Vice President for Research

Signature Date Date First Effective: Signature Date Revision Date:

Tuesday, May 15, Please be sure to sign in and take copies of each handout.

Transcription:

IORG #: IORG0001492 Institution: U of Cape Town Expires: 11/25/2018 OMB No. 0990-0279 Approved for use through October 31, 2018 U.S. Department of Health and Human Services (HHS) Registration of an Institutional Review Board (IRB) This form is used by institutions or organizations operating IRBs that review: a) Research involving human subjects conducted or supported by the Department of Health and Human Services, or other federal departments or agencies that apply the Federal Policy for the Protection of Human Subjects to such research; and/or b) Clinical investigations regulated by the Food and Drug Administration (FDA) of the Department of Health and Human Services This form is to be used for the following purposes: a. To register an IRB if your institution or organization has not previously registered an IRB b. To update or renew the registration of an IRB previously registered by your institution or organization c. To add another IRB to those previously registered by your institution or organization Fields with an * are required for OHRP IRBs and FDA IRBs Fields with an are required for OHRP IRBs but are optional for FDA IRBs Fields with an are required for FDA IRBs but are optional for OHRP IRBs Fields with no symbol are optional for both OHRP IRBs and FDA IRBs 1. *Has your institution or organization previously registered an IRB with the Office for Human Research Protections (OHRP)? [X] es, proceed to section 2 [ ] No, proceed to section 3 2. *What is your institution or organization (IORG) number? IORG0001492 This number was provided by OHRP the first time your institution or organization registered an IRB. If you do not know your IORG number, search for your institution or organization on the OHRP website at http://ohrp.cit.nih.gov/search/search.aspx or contact OHRP using the contact information at http://www.hhs.gov/ohrp/daqi-staff.html or by telephone at 1-866-447-4777. 3. Name of Institution or Organization Operating the IRB(s) *Name of Institution or Organization: U of Cape Town

*Mailing Address: Private Bag X3 Rondebosch 7700 *Street Address (if different from the Mailing Address above): Bremner Building Lovers Walk, Rondebosch 7701 *City: Cape Town *State/Province: *Zip/Postal Code: *Country (if outside the U.S.): SOUTH AFRICA 4. Senior Officer or Head Official of Institution or Organization Responsible for Overseeing the Activities Performed by the IRB(s) *First Name: Hugh Middle Initial: T *Last Name: Amoore Earned Degree(s): BA Title or Position: Registrar *Mailing Address (if different from the Mailing Address in section 3): Private Bag X3 Rondebosch 7701 South Africa Postcode 7701 *City: Cape Town *State/Province: *Zip/Postal Code: *Country (if outside the U.S.): SOUTH AFRICA *Phone: 27 21 650-2115/6 *FAX: 27 21 650-2138 *E-Mail: hugh.amoore@uct.ac. za 5. Contact Person Providing this Registration Information *First Name: Robert Middle Initial: H *Last Name: McLaughlin Earned Degree(s): JD, PhD Title or Position: Manager, Office of Research Integrity Name of Institution or Organization (if different from the Name in section 3): University of Cape Town *Mailing Address (if different from the Mailing Address in section 3): Allan Cormack House, 2 Rhodes Ave. Rm 220 Mowbray 7700 South Africa Postcode 7700 *City: Cape Town *State/Province: *Zip/Postal Code: *Country (if outside the SOUTH AFRICA

*Phone: 27 21 650-1946 *FAX: 27 21 650-5768 *E-Mail: robert.mclaughlin@ uct.ac.za 6. IRB Registration Information (to be completed separately for each IRB being renewed/updated or newly registered)

A. *Is this a renewal or update of a registration for an IRB already registered with HHS? [X] es. Provide the IRB registration number previously assigned to this IRB by OHRP: IRB00001937 (This number was provided by OHRP the first time the IRB was registered with OHRP. If you do not know the IRB registration number, search for the IRB on the OHRP website at http://ohrp.cit.nih.gov/search/search.aspx or contact OHRP using the contact information at http://www.hhs.gov/ohrp/daqi-staff.html or by telephone at 1-866-447-4777) [ ] No, this is a new IRB registration. B. Provide the IRB name, if any, used by the institution or organization (e.g., State University Behavioral IRB, University Healthcare Biomedical IRB, or XZ Hospital IRB #1): U of Cape Town IRB #1 - Senate Ethics in Rsch Committee C. Location of the IRB *Mailing Address (if different from the Mailing Address in section 3): Private Bag X3 Rondebosch 7701 *Street Address of the IRB (if different from the Mailing Address of the IRB): Bremmer Building Lovers Walk, Rondebosch 7701 *City: Cape Town *State/Province: *Zip/Postal Code: *Country (if outside the U.S.): SOUTH AFRICA *Phone: +27216502193 *FAX: +27216502138 *E-Mail: claude.bassuday@uct.ac.za D. Approximate number of full time equivalent positions devoted to the IRB s administrative activities: E. Approximate number of all active protocols (for purposes of completing this registration, an active protocol is any protocol for which the IRB conducted an initial review or continuing review at a convened meeting or under an expedited review procedure during the preceding 12 months): F. Approximate number of active protocols conducted or supported by HHS (e.g., the National Institutes of Health, Centers for Disease Control and Prevention, etc.) (for purposes of completing this registration, an active protocol is any protocol for which the IRB conducted an initial review or continuing review at a convened meeting or under an expedited review procedure during the preceding 12 months): 1 3 0

G. For IRBs that review, or intend to review, protocols involving products regulated by the Food and Drug Administration (FDA) (for purposes of completing this registration, an active protocol is any protocol for which the IRB conducted an initial review or continuing review at a convened meeting or under an expedited review procedure during the preceding 12 months): i) Approximate number of active protocols involving FDA-regulated products: ii) Types of FDA-regulated products involved in FDA protocols include (check all that apply): human drugs medical devices biological food additives color additives other Specify H. IRB Chairperson *First Name: Francois Middle Initial: *Last Name: Viruly Earned Degree(s): PhD Title or Position: Associate Professor Mailing Address (if different from the Mailing Address in section 3): Dept. Construction Engineering and Management Faculty of Engineering University of Cape Town Private Bag X3 Rondebosch 7701 City: Cape Town State/Province: Zip/Postal Code: Country (if outside the U.S.): SOUTH AFRICA *Phone: 27 21 650-3442 FAX: 27 21 650-5768 *E-Mail: francois.viruly@uct.ac.za

I. IRB Roster Form: Completion of the IRB Roster Form is required if your IRB is designated on a Federalwide assurance submitted to OHRP. Otherwise, it is optional. Member Name (Last, First) Sex M/F Earned Degree(s) Scientist (S) Non-scientist (N) N S Primary Scientific or Non-Scientific Specialty Affiliation with Institution(s) /N Comments Viruly, Francois F BA LLB Engineering Chair Blockman, Marc M MBChB, Clinical Medicine BPharm, MMed Cliff, Alan M PhD N Educational Assessment Seekings, Jeremy M BA(Hons), N Political Philosophy DPhil Hoffman, Paul M BA LLB N Law, N Advocate and external member Visser, Danie M B Juris, LLB, N Law Advocate and deputy vice chancellor LLD with research portfolio John-Langba, Johannes M Ph.D N Social Development Day, Jonathan M B.Sc(Med) S immunology Post graduate student representative Hons Berg, Julie F PhD N Law Hill, Richard M PhD S Environmental & Geographical Science London, Leslie M MD S Family Medicine & Public Health Walton, Marion F PhD S Film & Media Studies Rivett, Ulrike F PhD S Information Systems Sithole, George M PhD S Engineering Alternative Members NOTES: Members whose training, background, and occupation would incline them to view scientific activities from the standpoint of someone within a behavioral or biomedical research discipline should be considered a scientist, while members whose training, background, and occupation would incline them to view research activities from a standpoint outside of any biomedical or behavioral scientific discipline should be considered a nonscientist. In addition, the IRB must have members with sufficient knowledge of the specific scientific discipline(s) relevant to the research that it reviews. Affiliation: Please indicate whether or not each individual (or a member of that person s immediate family) is affiliated (other than as an IRB member) with the institution or organization operating the IRB. es = The IRB member is affiliated with the institution or organization operating the IRB.

No = The individual is not affiliated with the institution or organization operating the IRB. Alternate Members: An alternate member(s) may be designated, as needed, for a regular voting member(s). An alternate member may vote only when the regular voting member is not voting. When an institution or organization registers two or more IRBs, all alternate members for all IRBs may be listed on the roster of one IRB, or they may be listed separately with each IRB roster. A primary member of any IRB registered under the same IORG number may serve as an alternate for any comparably qualified member on any other IRB of that institution or organization. Primary members on registered IRBs serving as alternate members do not need to be listed as an alternate on any roster. Each alternate IRB member who replaces a primary member at any given meeting should have experience, expertise, background, professional competence, and knowledge comparable to that of the primary IRB member whom the alternate will replace. Whenever an alternate member substitutes for a primary member of the IRB, the combined requirements of 46.107(a) and 46.108(b) shall remain satisfied. Whenever this occurs, the minutes of the IRB meeting should indicate clearly that the alternate IRB member has replaced the designated primary IRB member, and include the identity of the replaced primary and the alternate members. If multiple alternate members serve at an IRB meeting, the pairing of primary and alternate members should be indicated.

A. *Is this a renewal or update of a registration for an IRB already registered with HHS? [X] es. Provide the IRB registration number previously assigned to this IRB by OHRP: IRB00001938 (This number was provided by OHRP the first time the IRB was registered with OHRP. If you do not know the IRB registration number, search for the IRB on the OHRP website at http://ohrp.cit.nih.gov/search/search.aspx or contact OHRP using the contact information at http://www.hhs.gov/ohrp/daqi-staff.html or by telephone at 1-866-447-4777) [ ] No, this is a new IRB registration. B. Provide the IRB name, if any, used by the institution or organization (e.g., State University Behavioral IRB, University Healthcare Biomedical IRB, or XZ Hospital IRB #1): U Cape Town IRB #2 - HS Rsch & Ethics Committee C. Location of the IRB *Mailing Address (if different from the Mailing Address in section 3): Private Bag X3 Lovers Walk Rondebosch, 7701 *Street Address of the IRB (if different from the Mailing Address of the IRB): Bremmer Building Lovers Walk, Rondebosch 7701 *City: Cape Town *State/Province: *Zip/Postal Code: *Country (if outside the U.S.): SOUTH AFRICA *Phone: +27216505828 *FAX: +27216502135 *E-Mail: claude.basuday@uct.ac.za D. Approximate number of full time equivalent positions devoted to the IRB s administrative activities: E. Approximate number of all active protocols (for purposes of completing this registration, an active protocol is any protocol for which the IRB conducted an initial review or continuing review at a convened meeting or under an expedited review procedure during the preceding 12 months): F. Approximate number of active protocols conducted or supported by HHS (e.g., the National Institutes of Health, Centers for Disease Control and Prevention, etc.) (for 2 3

National Institutes of Health, Centers for Disease Control and Prevention, etc.) (for purposes of completing this registration, an active protocol is any protocol for which the IRB conducted an initial review or continuing review at a convened meeting or under an expedited review procedure during the preceding 12 months): G. For IRBs that review, or intend to review, protocols involving products regulated by the Food and Drug Administration (FDA) (for purposes of completing this registration, an active protocol is any protocol for which the IRB conducted an initial review or continuing review at a convened meeting or under an expedited review procedure during the preceding 12 months): i) Approximate number of active protocols involving FDA-regulated products: ii) Types of FDA-regulated products involved in FDA protocols include (check all that apply): X X X human drugs medical devices biological food additives color additives other Specify 10 25 H. IRB Chairperson *First Name: Marc Middle Initial: *Last Name: Blockman Earned Degree(s): MD Title or Position: Associate Professor Medicine/IRB Chairperson Mailing Address (if different from the Mailing Address in section 3): Department of Pharmacology K45, Old Main Building Groote Schuur Hospital Observatory 7935 South Africa City: Cape Town State/Province: Zip/Postal Code: Country (if outside the U.S.): SOUTH AFRICA *Phone: 27 21 406-6496 FAX: 27 21 448-1989 *E-Mail: marc.blockman@uct.ac.za

I. IRB Roster Form: Completion of the IRB Roster Form is required if your IRB is designated on a Federalwide assurance submitted to OHRP. Otherwise, it is optional. Member Name (Last, First) Sex M/F Earned Degree(s) Scientist (S) Non-scientist (N) S S S Primary Scientific or Non-Scientific Specialty Affiliation with Institution(s) /N Comments Blockman, Marc M MD Pharmacology Ballo, Robea F BSc, PhD Human Genetics Coetzee, Minette F PhD, RSCN Child Nurse Practice Development Davids, Lester M PhD S Scientist Galetta, David, Rev. M Theologic N Theology N training Hunter, Alistair M PhD S Oncology Deputy Chair Lambert, Vicky F BA, PhD S Physical Education Pope, Anne F BA, LLB N Private Law Ross, Maureen F M CUR, RN S Nursing Management Wood, Robin M MBChB, S Infectious Diseases FCP Clow, Sheila F PhD, MSc, S Primary Scientific BSocSci Burgess, Theresa F PhD, Bsc S Physiotherapy Deputy Chair (Physiothera Colvin, Chris M PhD, MPH S Public Health & Family Medicine Joska, John M MBChB, S Psychiatry MMed (Psych), Myer, Landon M AB, MA, MPhil, MBChB S Public Health & Family Medicine Mowla, Shaheen F MD S haematology Naidoo, Lionel M MSc S health and rehabilitation Posthumus, Mike M PhD S human biology Schoeman, Leann F MD S obstetrics and gynaecology Peter, Jonny M MD S immunology Warden, Claire F MD S surgery Vusani, Nothemba F BA LLB N community health N organisations Blom, Dirk M MD S internal medicine Carrihill, Michelle F MD S paediatrics Cohen, Karin F MD S pharmacology Dandara, Collet F PhD S human genetics Duncan, Eve F D.Phil S occupational therapy

Kalula, Sebastiana F MD S geriatric medicine Morrow, Brenda F PhD S paediatrics Alternative Members NOTES: Members whose training, background, and occupation would incline them to view scientific activities from the standpoint of someone within a behavioral or biomedical research discipline should be considered a scientist, while members whose training, background, and occupation would incline them to view research activities from a standpoint outside of any biomedical or behavioral scientific discipline should be considered a nonscientist. In addition, the IRB must have members with sufficient knowledge of the specific scientific discipline(s) relevant to the research that it reviews. Affiliation: Please indicate whether or not each individual (or a member of that person s immediate family) is affiliated (other than as an IRB member) with the institution or organization operating the IRB. es = The IRB member is affiliated with the institution or organization operating the IRB. No = The individual is not affiliated with the institution or organization operating the IRB. Alternate Members: An alternate member(s) may be designated, as needed, for a regular voting member(s). An alternate member may vote only when the regular voting member is not voting. When an institution or organization registers two or more IRBs, all alternate members for all IRBs may be listed on the roster of one IRB, or they may be listed separately with each IRB roster. A primary member of any IRB registered under the same IORG number may serve as an alternate for any comparably qualified member on any other IRB of that institution or organization. Primary members on registered IRBs serving as alternate members do not need to be listed as an alternate on any roster. Each alternate IRB member who replaces a primary member at any given meeting should have experience, expertise, background, professional competence, and knowledge comparable to that of the primary IRB member whom the alternate will replace. Whenever an alternate member substitutes for a primary member of the IRB, the combined requirements of 46.107(a) and 46.108(b) shall remain satisfied. Whenever this occurs, the minutes of the IRB meeting should indicate clearly that the alternate IRB member has replaced the designated primary IRB member, and include the identity of the replaced primary and the alternate members. If multiple alternate members serve at an IRB meeting, the pairing of primary and alternate members should be indicated.

Public burden for this collection of information is estimated to average one hour for an initial IRB registration, and thirty minutes for updating or renewing the registration of a previously registered IRB. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to: OS Reports Clearance Officer, Room 503, 200 Independence Avenue, SW., Washington, DC 20201. Do not return the completed form to this address.