Eighth Edition - R.3 - Human Fertilisation & Embryology Authority

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HFEA guidance (cont) Notification of withdrawal of consent to parenthood (cont) Interpretation of mandatory requirements If a person withdraws their consent to being treated as the legal parent of any child resulting from the treatment of their partner, the person responsible (PR) must notify the partner in writing of this. The partner must not be treated with sperm and eggs, or with embryos, or be inseminated, until she has been notified in this way. If a woman withdraws her consent to her partner being treated as the legal parent of any child resulting from the woman’s treatment, or notifies the centre that she wishes a different person to be treated as the legal parent of any child resulting from her treatment, the PR must notify the partner in writing of this. Consent can be withdrawn only before sperm and egg or embryo transfer, or insemination. 6J 6.14 The PR should ensure that the written notification they issue explains and refers to the relevant parts of the legislation regarding legal parenthood and withdrawal of consent. See also: HFEA consent forms available at www.hfea.gov.uk Human Fertilisation and Embryology Authority Guidance note | 6. Legal parenthood Version 1.0
7. Multiple births This guidance note contains: Mandatory requirements • Reference to relevant HFEA Directions HFEA guidance • Strategy to minimise multiple births • Limits on egg and embryo transfer • Consent and provision of information Other legislation, professional guidelines and information Refer to principles 5, 6, 7, 10 and 13 Section includes interpretation of mandatory requirements Mandatory requirements Directions 0003 – Multiple births For a copy of the relevant Directions visit www.hfea.gov.uk HFEA guidance Strategy to minimise multiple births Interpretation of mandatory requirements HFEA Directions require centres to have a documented strategy to minimise multiple births. Its purpose is to reduce the annual rate of multiple births resulting from treatments at the centre. 7A The strategy must set out: (a) (b) (c) how the centre aims to reduce the annual multiple birth rate following treatment at that centre, and to ensure the rate does not exceed the maximum rate specified by the Authority as set out in Directions, the circumstances in which the person responsible would consider it appropriate to recommend single embryo transfer (SET) to a patient (in setting out such circumstances, the centre should give proper consideration to relevant professional guidance), and the criteria for transferring eggs during gamete intrafallopian transfer (GIFT). The centre must document regular audits that: (a) (b) assess progress in reducing its multiple birth rate, and help evaluate the effectiveness of its strategy. Human Fertilisation and Embryology Authority Guidance note | 7. Multiple births Version 1.0 2.0
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Code of Practice 8TH EDITION This C
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Contents User guide to the Code Reg
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Contents Facilities and administrat
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User guide to the Code Guidance not
Page 9 and 10: 1. Person responsible This guidance
Page 11 and 12: XX. Title of Guidance Note Mandator
Page 13 and 14: 2. Staff This guidance note contain
Page 15 and 16: v HFEA guidance (cont) 2.3 All staf
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Page 19 and 20: 3. Counselling This guidance note c
Page 21 and 22: = HFEA guidance (cont) Interpretati
Page 23 and 24: 4. Information to be provided prior
Page 25 and 26: HFEA guidance (cont) Interpretation
Page 27 and 28: 5. Consent to treatment, storage, d
Page 29 and 30: Mandatory requirements (cont) Proce
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Page 35 and 36: HFEA guidance (cont) Additional con
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Mandatory requirements (cont) Direc
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HFEA guidance (cont) 15.4 Sperm sho
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HFEA guidance (cont) Processing and
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HFEA guidance (cont) 15.16 (cont) (
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Mandatory requirements (cont) (4) D
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HFEA guidance (cont) General Direct
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17. Storage of gametes and embryos
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Mandatory requirements (cont) (2) N
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Mandatory requirements (cont) (3) (
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Mandatory requirements (cont) (b) e
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v HFEA guidance (cont) 17.10 In add
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v HFEA guidance (cont) Mandatory re
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18. Witnessing and assuring patient
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HFEA guidance (cont) 18.4 (cont) (j
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HFEA guidance (cont) 18.24 Centres
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HFEA guidance (cont) Risk assessmen
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Mandatory requirements (cont) T99 (
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20. Donor-assisted conception This
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v HFEA guidance (cont) See also gui
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HFEA guidance (cont) 20.11 (cont) (
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22. Research and training This guid
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Mandatory requirements (cont) (3) A
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Mandatory requirements (cont) (3) W
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Mandatory requirements (cont) T95 T
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HFEA guidance (cont) Information pr
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HFEA guidance (cont) Consent Interp
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HFEA guidance (cont) Mandatory requ
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HFEA guidance (cont) Interpretation
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HFEA guidance (cont) Human admixed
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XX. Title of Guidance Note Mandator
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HFEA guidance (cont) 23.10 Centre m
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XX. Title of Guidance Note HFEA gui
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24. Third party agreements This gui
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Mandatory requirements (cont) T117
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25. Premises and facilities This gu
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HFEA guidance Definition of premise
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26. Equipment and materials This gu
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HFEA guidance (cont) See also guida
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Mandatory requirements (cont) Licen
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HFEA guidance (cont) 27.4 A ‘near
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28. Complaints This guidance note c
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29. Treating people fairly This gui
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HFEA guidance (cont) 29.9 Staff at
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30. Confidentiality and privacy Thi
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Mandatory requirements (cont) (j) (
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Mandatory requirements (cont) 35 Di
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HFEA guidance (cont) 30.7 A person
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HFEA guidance (cont) Consent to dis
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31. Record keeping and document con
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Mandatory requirements (cont) T40 T
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v HFEA guidance (cont) 31.4 (cont)
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Mandatory requirements (cont) Seizu
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HFEA guidance Legal obligations tow
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Glossary D Data subject: Defined by
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Glossary N Near miss: Any occurrenc
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Glossary S Serious adverse reaction
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Index C carrier embryos, transfer o
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Index donation for research/trainin
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Index of justification for use of g
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Index charges and benefits 12.20 co
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Index embryonic stem cells/lines se
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Index preimplantation tissue typing
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Index L labelling dishes and tubes
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Index likely, information provision
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Index identification of processes n
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Index licence R25(22), 22A, 22.1 An
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Index additional requirements 5D, 5
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Index communication barrier handlin
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Eighth Edition - R.3 - Human Fertilisation & Embryology Authority

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