Medical Research

The Mission of the Center for Cardiovascular Diseases and Sciences (CCDS) Is to Reduce

The Mission of the Center for Cardiovascular Diseases and Sciences (CCDS) Is to Reduce

The mission of the Center for Cardiovascular Diseases and Sciences (CCDS) is to reduce the impact of cardiovascular/cerebrovascular disease through research and clinical practice. The CCDSrecognizes the beneficial role of interdisciplinary partnerships.

Call for Applications/Proposals 2013Self-Initiated Research Category

Call for Applications/Proposals 2013Self-Initiated Research Category

Dear Heads of Departments, Departmental Research Chairs, Directors of Research Units & Researchers. CALL FOR APPLICATIONS/PROPOSALS 2013SELF-INITIATED RESEARCH CATEGORY. Health researchers are invited to submit applications/proposals for funding under.

Rutgers Biomedical and Health Sciences (Rbhs)

Rutgers Biomedical and Health Sciences (Rbhs)

RUTGERS BIOMEDICAL AND HEALTH SCIENCES (RBHS). EXTRAMURAL SUPPORT INCENTIVE PROGRAM - FY2017. FOR FACULTY IN THE AAUP-BHSNJ NEGOTIATIONS UNIT. PART A TO BE COMPLETED BY FACULTY MEMBER.

Clinical Trial Notification Details Form

Clinical Trial Notification Details Form

CLINICAL TRIAL NOTIFICATION DETAILS FORM. Initial notification (complete all sections of the form). Change to existing notification (only complete the sections which have changed). SITE CONTACT DETAILS. 1.2 Contact phone number.

Registering Clinical Trials at Nova Scotia Health Authority (NSHA)

Registering Clinical Trials at Nova Scotia Health Authority (NSHA)

Registering Clinical Trials at Nova Scotia Health Authority (NSHA). Clinical trial registration numbers are required at NSHA for all relevant research ethics submissions. This number is a result of publicly registering the clinical trial on a recognized website (. Why register a trial?

Investigational Drug Study Registry Form

Investigational Drug Study Registry Form

INVESTIGATIONAL DRUG STUDY REGISTRY FORM. DEPARTMENT OF PHARMACEUTICAL AND NUTRITION CARE. THE NEBRASKAMEDICALCENTERHOSPITAL AND CLINIC. AND UNIVERSITY OF NEBRASKAMEDICALCENTER. To maintain compliance with both Medical Staff Policy No. 5 III and the.

Additional File 1 Representative Search Strategy

Additional File 1 Representative Search Strategy

Additional file 1 Representative Search Strategy. Database: Embase Classic+Embase <1947 to 2013 June 05>, Ovid MEDLINE(R) In-Process & Other Non-Indexed Citations and Ovid MEDLINE(R) <1946 to Present> Search Strategy. 1 Mesenchymal Stem Cells/ (34040).

IRB Reviewer Form: Appendix C(Children)

IRB Reviewer Form: Appendix C(Children)

IRB Reviewer Form: Appendix C(Children). Control/Placebo Group (if applicable): Select the risk category for the child participants that will be in a control/placebo group. Parental Permission. The waiver will not adversely affect the rights and welfare of the child.

FWA IRB00006183; IRB 00000447; IORG 0000264; U Virginia IRB#1

FWA IRB00006183; IRB 00000447; IORG 0000264; U Virginia IRB#1

FWA IRB00006183; IRB 00000447; IORG 0000264; U Virginia IRB#1. Update of Membership Roster Only. UNIVERSITY OF VIRGINIA. INSTITUTIONAL REVIEW BOARD-HEALTH SCIENCES RESEARCH (IRB-HSR). Richard Stevenson, MD. Scientist/Affiliated. Amy P. Adams, Pharm D.

Study 1: Black MSM in Africa: a Behavioral Feasibility Study for Recruitment, Retention

Study 1: Black MSM in Africa: a Behavioral Feasibility Study for Recruitment, Retention

Study 1: Black MSM in Africa: A behavioral feasibility study for recruitment, retention, and measurement of social impacts. General Site Information (Research Experience/ Network Affiliation/ Recruitment/Retention/ Regulatory) (40% of total score) (LOC votes on this category).

Please Attach Electronic Files of All Documents (6.1 6.20)

Please Attach Electronic Files of All Documents (6.1 6.20)

Please fill in this form and provide necessary documents for submission. This form will help expedite the review process. Note: หลังจากยื่นเอกสารผ่านทางระบบออนไลน์และได้รับIRB No. แล้วInvestigator has to provide document 6.1, 6.3-6.9, 6.11-6.12 and 1.

RFI: Consortia RFA

RFI: Consortia RFA

The purpose of this Request for Information (RFI) is to gather feedback from scientists, clinicians and administrators who have experience working in multi-institutional research programs (hereafter referred to as consortia ). The information gathered.

For Initial Review Using the Expedited Procedure, Modifications, and Continuing Reviews

For Initial Review Using the Expedited Procedure, Modifications, and Continuing Reviews

For initial review using the expedited procedure, modifications, and continuing reviews where the determinations relevant to this checklist made on the previous review have changed, the Designated Reviewer completes this checklist to document determinations.

Clinical Governance Is a System Through Which NHS Organisations Are Accountable for Continuously

Clinical Governance Is a System Through Which NHS Organisations Are Accountable for Continuously

PROMOTING AND MAINTAINING. HIGH STANDARDS OF. CLINICAL CARE. FOR OUR PATIENTS. Scally and Donaldson 1998 defined clinical governance as a system widely used within the NHS as a means whereby organisations are accountable for continuously improving the.

Self Reporting Monitoring Form

Self Reporting Monitoring Form

For Observational Studies this form is for information only. No action is required but we suggest you use this as guidance to ensure all aspects of your study are compliant with Good Clinical Practice.

2008-2009 Irb Meeting Dates & Deadlines

2008-2009 Irb Meeting Dates & Deadlines

2017 IRB MEETING DATES & DEADLINES. I M P O R T A N T Please Read. These deadlines apply to ALL applications submitted for IRB/SRS/R&D review and approval, including, but is not limited to, Initial Review, Continuing Review, Closure, Amendments, Adverse Events, etc.

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