Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 15 (5) (d)

Document information
Reference	GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
Validity area	GBR
Scope(s)	HM
Document name	The Medicines for Human Use (Clinical Trials) Regulations 2004
Version / Revision	01-May-2004
Status	Current
Document type	Legal act
Language(s)	EN
Description	The Medicines for Human Use (Clinical Trials) Regulations 2004
Official source	Official link
Restricted access	No
Submitted by	Florian Adragna
Contributors

Reference Details
Module	Module 2 — Unit 2.3.3
Scope	HM
Document part	Article 15 (5) (d)
Language	EN
Original entry by	Florian Adragna
Contributors
Tags	Ethics committee, Investigator, Site staff

Content

Ethics committee opinion 15.— [...] (5) In preparing its opinion, the committee shall consider, in particular, the following matters—

(d)the suitability of the investigator and supporting staff;