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Changes over time for: Section 2
Llinell Amser Newidiadau
This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.
Version Superseded: 31/12/2020
Status:
Point in time view as at 28/10/2011. This version of this provision has been superseded.
Status
You are viewing this legislation item as it stood at a particular point in time. A later version of this or provision, including subsequent changes and effects, supersedes this version.
Note the term provision is used to describe a definable element in a piece of legislation that has legislative effect – such as a Part, Chapter or section.
Changes to legislation:
There are currently no known outstanding effects for the The Blood Safety and Quality Regulations 2005, Section 2.
Changes to Legislation
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Designation of the competent authority and scope of the RegulationsU.K.
This
adran has no associated
Memorandwm Esboniadol
2.—(1) The Secretary of State is designated the competent authority for the purpose of the Directive.
(2) Subject to the following paragraphs, the requirements of these Regulations apply to the collection and testing of blood and blood components, whatever their intended purpose, and to their processing, storage, and distribution when they are intended to be used for transfusion.
(3) These Regulations apply without prejudice to the Medical Devices Regulations 2002 .
(4) These Regulations do not apply to blood stem cells.
Yn ôl i’r brig