Guide: How to cite a Report in Harvard - Imperial College London style

Guide: How to cite a Report in Harvard - Imperial College London style

Cite A Report in Harvard - Imperial College London style

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Use the following template to cite a report using the Harvard - Imperial College London citation style. For help with other source types, like books, PDFs, or websites, check out our other guides. To have your reference list or bibliography automatically made for you, try our free citation generator.

Key:

Pink text = information that you will need to find from the source.
Black text = text required by the Harvard - Imperial College London style.

Reference list

Place this part in your bibliography or reference list at the end of your assignment.

Template:

Author Surname, Author Initial. (Year Published) Title. [Online].  p.Pages Used. Available from: http://Website URL [Accessed: Date Accessed].

Example:

European Medicines Agency, (2010) European Medicines Agency 7 Westferry Circus, Canary Wharf, London, E14 4HB, UK Tel. (44-20) 74 18 84 00 Fax (44-20) 74 18 86 13 E-mail: mail@ema.europa.eu http://www.ema.europa.eu © European Medicines Agency, 2010. Reproduction is authorised provided the source is acknowledged. London, 20 January 2010 Doc. Ref.: CPMP/EWP/QWP/1401/98 Rev. 1/ Corr ** COMMITTEE FOR MEDICINAL PRODUCTS FOR HUMAN USE (CHMP) GUIDELINE ON THE INVESTIGATION OF BIOEQUIVALENCE.  pp.1 - 27; http://www.tga.gov.au/industry/pm-euguidelines-adopted-clinical.htm#.U7JLOLGBlcq.

In-text citation

Place this part right after the quote or reference to the source in your assignment.

Template

(Author Surname, Year Published)

Example

This guideline  is available on the TGA website under the heading: Clinical pharmacology and pharmacokinetics. The TGA notes under the link to the reference  that "While this guidance suggests that the design and conduct of the study should follow EU regulations on Good Clinical Practice, sponsors should note that the EU Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95) has been adopted in Australia with TGA annotations.
The procedure for abridged applications claiming essential similarity to a reference product (i.e., generics), which allows applications to be made to numerous Member States of the EU, based on bioequivalence with a reference product from one Member State, does not apply in Australia. An application for registration of a generic product in Australia should generally include a bioequivalence study versus a leading brand obtained in Australia." (European Medicines Agency, 2010)

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