References

References and Useful Links

Legislation and MOH Resources	Human Biomedical Research Act 2015
Legislation and MOH Resources	MOH HBRA Decision Tools - Is my study Human Biomedical Research? - Am I handling human tissue and conducting tissue banking activities regulated under the Human Tissue Framework?
Related Offices and Sites in NUS	Office of Deputy President (Research & Technology)
	NUS Life Sciences Institute
	Office of Safety, Health & Environment
	NUS Institutional Animal Care & Use Committee
Organisations	Bioethics Advisory Committee (BAC)
	Health Sciences Authority (HSA)
	Ministry of Health (MOH) ***MOH guidelines on the Human Biomedical Research Act
	Singapore Medical Association (SMA)
	NHG Domain Specific Review Boards (NHG DSRBs)
	Singhealth Centralized Institutional REview Board (CIRB)
Research Institutes	National Medical Research Council (NMRC)
Research Institutes	Agency for Science, Technology and Research (A*STAR):
Hospitals	Alexandra Hospital (AH)
	Changi General Hospital (CGH)
	Institute of Mental Health (IMH)
	KK Women's & Children's Hospital (KKH)
	National University Hospital (NUH)
	Singapore General Hospital (SGH)
	Tan Tock Seng Hospital (TTSH)
	Khoo Teck Puat Hospital (KTPH)

The American Journal of Bioethics Online	International Compilation of Human Research Standards
Australian National Health and Medical Research Council	U.S. Office of Human Research Protections (OHRP)
CIOMS - International Ethical Guidelines For Epidemiological Studies (2008)	U.S. National Institute of Health (NIH)
European Forum for Good Clinical Practice (EFGCP)	World Medical Association (WMA)
International Bioethics Centre, UNESCO	Global Forum for Health Research
Johns Hopkins University Bioethics Institute, USA	World Health Organization (WHO)
Food and Drug Administration (FDA) -Information Sheet Guidances -Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors

AAHRPP-Accreditation Procedures	IBC-Universal Declaration on the Human Genome
Belmont Report	ICMJE-Sponsorship, Authorship, and Accountability (2002)
Biomedical Ethics in U.S. Public Policy	IOM-Preserving the Public Trust
BMJ-Clinical Guidelines-Benefits and Limits	2019-International-Compilation-of-Human-Research-Standards
CIOMS - International Ethical Guidelines For Epidemiological Studies (2008)	Medicines Act [Chap. 176]
Code of Federal Regulations Title 21 Part 56 (CFR 21-56)	Medicines (Clinical Trial Regulations), 2016
Code of Federal Regulations Title 45 Part 46 (CFR 45-46)	NIAID-DSMB Guideline
Declaration of Helsinki	Nuremberg
Detailed Guidance on the European CT Database	OIG-Globalization of Clinical Trials
EFGCP-Guidelines and Recommendations 1997	OIG-Tissue Banking (Jan 2001)
Ethical Considerations in HIV Preventive Vaccine Research (UNAIDS-Guidance Document 2000)	Personal Data Protection Act (2012)
European Directive 2001	Terms of the FWA
FDA Acceptance of Foreign Clinical Studies	Tuskegee Syphilis Study
FDA-Computerized Systems Used in Clinical Trials (2007)	WHO Declaration of Interests for WHO Experts
FDA-Draft Guidance on CT DMCs (2006)	WHO-Defining Policy through Action
FDA-Testing Drugs in People 1995	WHO GCP 1995
Guidance for Industry E6 Good Clinical Practice: Consolidated Guidance 1996 (ICH-GCP E6)	WHO-Operational Guidelines (2000)