Institutional Review Board (IRB)

Review all research that involves human subjects to ensure adherence to ethical standards.

 
Chair: Frances García
fgarcia@uccaribe.edu
 

Members

 
Wanda Figueroa, M.D.
Frances García, M.D.
Zahira Lespier, Ph.D.
Gerónimo Maldonado, Ph.D.
Karla Narváez, Ph.D.
Carlos Nazario, B.A.
Juan L. Negrón, Ph.D.
José Ramírez, M.D.
Yomarie Rivera-Román, Ph.D.
Vidal Vélez, Ph.D., M.A.
 
 

Forms and Regulations

IRB Fee Services

IRB Application Form Rev. May 2019

Protocol Identification Universal Number Form

IRB Recommendations for the protection during the COVID-19 pandemic

REVISED COMMON RULES, EFFECTIVE JANUARY 21, 2019
(https://www.govinfo.gov/content/pkg/FR-2017-01-19/pdf/2017-01058.pdf)

UCC- 2018 FEDERAL POLICY FOR THE PROTECTION OF HUMAN SUBJECTS (45 CFR 46)- RULES AND REGULATIONS 2018

RESUMEN – 2018 FEDERAL POLICY FOR THE PROTECTION OF HUMANS SUBJECTS- 45 CFR 46 – RULES AND REGULATIONS 2018

IRB Comunicado

IRB Guide for the Creation of HIPAA Documentation 2013

HIPAA Form for Investigations

Human Subject Regulations Decision Charts

Food and Drug Administration

Human Research Protections

45CFR46 Protection of Human Subjects

“WHO NEEDS: TRAINING ON THE NIH´S CHANGES TO CLINICAL TRIALS POLICIES-  GOOD CLINICAL PRACTICE (GCP) TRAINING”.  https://grants.nih.gov/grants/guide/notice-files/NOT-OD-16-148.html, https://grants.nih.gov/policy/clinical-trials/good-clinical-training.htm

 

Web Certificate

Link to get Web Certificates go to https://about.citiprogram.org/en/homepage/
Certificados de Human Subjects Research (HSR), Information Privacy & Security (IPS) & Good Clinical Practice (GCP)