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There are outstanding changes not yet made by the legislation.gov.uk editorial team to The Human Tissue (Quality and Safety for Human Application) Regulations 2007. Those changes will be listed when you open the content using the Table of Contents below. Any changes that have already been made by the team appear in the content and are referenced with annotations.
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Whole provisions yet to be inserted into this Instrument (including any effects on those provisions):
PART 2 LICENSING OF ACTIVITIES RELATING TO THE USE OF TISSUE FOR HUMAN APPLICATION
PART 4 OBLIGATIONS OF THE AUTHORITY
19.Register of serious adverse events and serious adverse reactions
20.Duties of the Authority in relation to serious adverse events and serious adverse reactions
20A.Duties of the Authority in relation to application of the Single European Code in relation to Northern Ireland
20B.Inspection of third country premises etc , Northern Ireland
20C.Third country premises and third country suppliers: report of inspections etc , Northern Ireland
Directions for securing compliance with the first, second, third and fourth Directives
Third party agreements and termination of licensed activities
Selection criteria and laboratory tests required for donors of tissues and cells
Donation and procurement procedures and reception at the tissue establishment
Requirements for holding a licence under Schedule 1 for tissue and cell preparation processes
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