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Human Fertilisation and Embryology Act 1990 is up to date with all changes known to be in force on or before 15 September 2024. There are changes that may be brought into force at a future date.
Revised legislation carried on this site may not be fully up to date. Changes and effects are recorded by our editorial team in lists which can be found in the ‘Changes to Legislation’ area. Where those effects have yet to be applied to the text of the legislation by the editorial team they are also listed alongside the affected provisions when you open the content using the Table of Contents below.
The Human Fertilisation and Embryology Authority, its functions and procedure
13A.Conditions of licences for non-medical fertility services
15A.Duties of the Authority in relation to serious adverse events and serious adverse reactions
15B.Inspection of third country premises etc.: Northern Ireland
15C.Third country premises and third country suppliers: report of inspections etc: Northern Ireland
Grant, revocation and suspension of licences
31ZC.Power of Authority to inform donor of request for information
31ZD.Provision to donor of information about resulting children
31ZE.Provision of information about donor-conceived genetic siblings
31ZG.Financial assistance for person setting up or keeping voluntary contact register
31B.The Authority's register of serious adverse events and serious adverse reactions
33C.Power to provide for additional exceptions from section 33A(1)
33D.Disclosure for the purposes of medical or other research
35. Disclosure in interests of justice: congenital disabilities, etc.
SCHEDULES
Consents to use OR STORAGE OF GAMETES, EMBRYOS OR HUMAN ADMIXED EMBRYOS ETC
CIRCUMSTANCES IN WHICH OFFER OF COUNSELLING REQUIRED AS CONDITION OF LICENCE FOR TREATMENT
SUPPLEMENTARY LICENCE CONDITIONS: HUMAN APPLICATION
Serious adverse events and serious adverse reactions : Great Britain
Serious adverse events and serious adverse reactions: Northern Ireland
Third party agreements and termination of licensed activities
Selection criteria and laboratory tests required for donors of reproductive cells
Donation and procurement procedures and reception at the tissue establishment
Requirements for holding a licence under paragraph 1, 1A or 2 of Schedule 2
Requirements for holding a licence for gametes and embryo preparation processes
Requirements where gametes or embryos imported from third country
Inspection, entry, search and seizure
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