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.
Juan L. Negrón, Ph.D.
José Ramírez, M.D.
Vidal Vélez, Ph.D., M.A.
 
 

Forms and Regulations

For access the new 2018 rules and regulations in details, please go here: https://www.federalregister.gov/documents/2017/01/19/2017-01058/federal-policy-for-protection-of-human-subjects

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

Protocol Identification Universal Number Form

IRB Application Form Rev. Feb 2018

IRB Rules and Regulations Manual

IRB Guide for the Creation of HIPAA Documentation 2013

Institutional Review Board Guidebook

HIPAA Form for Investigations

Human Subject Regulations Decision Charts

Food and Drug Administration

Human Research Protections

45CFR46 Protection of Human Subjects

21 CFR 50 Protection of Human Subjects

Guidance on 45 CFR 46 PROTECTION OF HUMAN SUBJECTS

“WHO NEEDS: TRAINING ON THE NIH´S CHANGES TO CLINICAL TRIALS POLICIES-  GOOD CLINICAL PRACTICE (GCP) TRAINING”.

 

Web Certificate

Protecting Human Research Participants

Research Aspects of HIPAA

Good Clinical Practice (Researchers)