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Office of Research & Graduate Studies
Policies Procedures and Guidelines
> Research Policies
and Procedures
> Research Priorities
> Proposal
Submission Guidelines
> Research Compliance
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| Office of Research | News | Directory |
The Office of Research is responsible for ensuring compliance with the
regulations of Alfaisal University. The following guidelines are to assist
Faculty in preparing research proposals as well as providing an overview of the
processes and procedures followed during application & award phases.
Faculty must comply with relevant statutes or regulations for the protection and
welfare of researchers, human subjects, the public, laboratory animals and the
environment. Research involving the use of Biohazardous Material, Human and/or
Animal Subjects must be submitted to the appropriate Committee(s) for review and
approval. Funding will not be granted for research which has not been approved.
Medical research is subject to ethical standards that promote respect for all
human beings and protect their health and rights (World Medical Association
Declaration of Helsinki 2000).
Approval for research involving Human Subjects can not be initiated prior to
application and submission of related documentation and consent forms to the
designated Ethics Committee at the facility where the research will be
conducted.
Approval is granted for a specified duration and must be renewed to ensure
continuation of research. It is the responsibility of the Principal Investigator
to submit a progress report in accordance to the Committee guidelines for review
and approval. In some instances, projects that have not obtained approval before
the expiration date are terminated.
Any modifications to a research protocol, consent forms, or administrative
matters in addition to reporting of adverse events must be submitted for
approval by the Principal Investigator to the respective Committee(s).
Research involving the use of animals is subject to compliance of ethical
practices and standards which ensure their proper care, use and humane
treatment. Approvals must be obtained from the External Review Board (ERB)
available at each collaborating facility were the proposed research will take
place. The ERB is responsible for reviewing and approving all research
activities involving the use of animal subjects before a project is initiated.
Research which does not receive approval from the ERB will not be funded.
Laboratories are maintained by the facility administration that regulates and
ensures compliances to its rules and regulations. A link to the policies for each collaborative facility
is available in the University’s website.
It is the duty of faculty members conducting research to take necessary measures
to promote and secure safe and healthy working practices and environments. Use
of rDNA, biohazardous materials, or other agents must be detailed in the
research protocol. Review and approval must be obtained from respective
committees in facilities where the proposed work will take place. Proposals that
have not received prior approval will not be recommended for funding.
The following links outline essential local and international standards for
patents, intellectual property, and research compliance for research involving
human subjects; animal subjects, rDNA, and biohazardous material:
The Saudi Patent & Intellectual Property Law
National Committee for Biological and Medical Ethics