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Organizational Chart
(Spanish Version)
Calendar 2009-2010
(Spanish Version)
IRB Multiple Project Assurance
(PDF)
Consents Templates
Informed Consent Document
Consentimiento Informado
(Spanish Version) New Version
Informed Consent Evaluation Checklist
Helpful Documents
Suggested Outline of a Proposal for an Intramural Research Study
"Hoja para Comunicado de Prensa"
Before Submitting a Proposal to the IRB
Submitting a Research Project to Western IRB
Glosarry of Clinical Trials Term
Good Clinical Practice
Lay Terms
Policies
Policies and Procedures(NEW)
Policies and Procedures(old)
Report of Adverse Events
Audit Standard of Procedures
Guidelines for the Protection of Children
Investigator's Responsibilities
Policies for the Use of Reseach Biological Material
Certification 45 2006 2007 Scientific Misconduct
Circular Letter 96-03-1996 Conflict of Interest
Forms
HIPAA-use of identifiers
IRB Wise Account Request Personal Information
"Formulario para Miembros Activos"
(Spanish Version)
"Formulario para candidatos para los comités de IRB"
(Spanish Version)
Notices and Updates
Useful Links
Frequently Asked Questions
(Spanish Version)
Contact Information
IRBWise
IRBWise Manual
IRB Members
Useful Links
IRBWise:
http://irb.rcm.upr.edu
Western IRB:
http://www.wirb.com
OHRP:
http://www.hhs.gov/ohrp/
FDA:
http://www.fda.gov/
IND applications:
http://www.fda.gov/cder/regulatory/applications
Bioethics NIH:
http://www.bioethics.nih.gov/
CITI Course
(Human Subjects Protection, HIPAA , GCP training):
http://www.citiprogram.org/