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The Medicines for Human Use (Clinical Trials) Amendment Regulations 2006
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- UK Statutory Instruments
- 2006 No. 1928
- Regulation 4
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Insertion of regulation 3A of the principal Regulations
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4. After regulation 3 of the principal Regulations (sponsor of a clinical trial) insert the following regulation—
“Sponsor’s responsibility for the investigator’s brochure
3A. The sponsor of a clinical trial shall—
(a)ensure that the investigator’s brochure for that trial, and any update of that brochure, presents the information it contains in a concise, simple, objective, balanced and non-promotional form that enables a clinician or potential investigator to understand it and make an unbiased risk-benefit assessment of the appropriateness of the proposed clinical trial; and
(b)validate and update the investigator’s brochure at least once a year.”.
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