Official guidelines on clinical trials

	A Standard for the Scientific and Ethical Review of Trials (ASSERT)
	Australian Therapeutic Goods Administration
	CancerIndex
	Cancernet.co.uk
	Central Committee on Research Involving Human Subjects (CCMO)
	Clinical Trials Tool Kit
	Community of Science
	European Agency for the Evaluation of Medicinal Products (EMEA)
	European Clinical Trials Directive 2001/20/EC
	Heads of EU Agencies Website
	International Committee of Medical Journal Editors (ICMJE) - Uniform Requirements for Manuscripts Submitted to Biomedical Journals
	International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use - Guideline for Good Clinical Practice (ICH GCP)
	International Directory of Government and Regulatory Bodies (Pharmweb)
	James Lind Library
	Medical Dictionary for Regulatory Activities Terminology (MedDRA)
	PhRMA New Medicines in Development Database
	The Cochrane Collaboration
	The CONSORT Statement
	The Quality Of Reporting Of Meta-analyses (QUOROM) Statement
	The UK Medicines and Healthcare products Regulatory Agency (MHRA)
	UK Central Office for Research Ethics Committees (COREC)
	UK Department of Health Policy and Guidance on Research and Development
	UK National Library for Health
	US Food and Drug Administration (FDA)
	US National Institutes of Health (NIH): Institutes, Centers & Offices
	US Office for Human Research Protections (OHRP)
	WHO Guidelines for Good Clinical Practice for Trials on Pharmaceutical Products
	WHO International Clinical Trials Registry Platform (ICTRP)
	WHO operational guidelines for ethics committees that review biomedical research
	World Medical Association Declaration of Helsinki

October 2007