Fertility clinics to provide patients with costed treatment plans under fertility regulator’s new Code of Practice

07 July 2009

Fertility clinics will be expected to provide every patient with a costed treatment plan, under new guidelines for UK fertility clinics published today.

Costed treatment plans are just one of the changes set out in the Human Fertilisation and Embryology Authority’s (HFEA) 8th Code of Practice for fertility clinics which comes into effect with the Human Fertilisation and Embryology Act 2008 on 1 October 2009. Costed treatment plans set out how much treatment will cost before it starts.

Plans will be updated if the costs change during the course of treatment.

Other key changes to the Code include:

  • a clear definition of supportive parenting to help them make a welfare of the child assessment before carrying out treatment
  • a cooling-off period for couples who have parted but who have embryos in storage allowing time for former partners to come to a reconciliation
  • bringing the HFEA’s long standing ban on sex selection for non-medical or ‘social’ reasons into law.

Professor Lisa Jardine CBE, Chair of the HFEA, said,

“With the majority of people in the UK funding their own treatment, cost is a major concern. The changes to our Code will help ensure that patients know upfront exactly how expensive their treatment will be.

“The UK’s fertility clinics treat thousands of patients each year and are responsible for the safety of these patients, their eggs, sperm and embryos.  Our new Code of Practice sits alongside robust and targeted regulation, to ensure that clinics are absolutely clear about their responsibilities. “

Ends

 

Notes to editors

  • The 8th Code, is available in PDF format on the HFEA website – www.hfea.gov.uk/get-ready 
  • The HFEA’s 8th Code of Practice sets out the standards under which fertility clinics operate in the UK.  Developed following consultation with professionals and patients, the new Code helps clinics meet new legal requirements and introduces some changes in response to feedback from patients and licensed clinics. 
  • It will come into force on 1st October 2009, when the bulk of the updated Human Fertilisation and Embryology Act takes effect. It is being published today to allow time for clinics to make the necessary changes to their procedures before 1st October.  For details of the three stages of commencement for the HFE Act 2008 see: http://www.hfea.gov.uk/134.html 
  • The HFEA carried out a consultation on the draft Code of Practice and consent forms between November 2008 and February 2009
  • The HFEA is the independent regulator for IVF treatment and embryo research. Our role is to protect patients and the public interest, to drive improvement in the treatment and research sectors and to provide information to the public and policymakers about treatment and research.
  • The HFEA was set up in August 1991 under of the Human Fertilisation and Embryology Act 1990. The HFEA’s principal tasks are to license and monitor clinics that carry out in vitro fertilisation (IVF), artificial insemination (AI) and human embryo research. The HFEA also regulates the storage of gametes (eggs and sperm) and embryos.

For further information contact the HFEA press office on 020 7291 8226 or email press.office@hfea.gov.uk 

Page last updated: 07 July 2009