• Directions
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• Multiple Births Minimisation Strategy: achievements and compliance
• Frequently used guidance
• Do I need to be registered by either the CQC or licensed by the HTA?
• Retrieval of storage of gametes where patients are unable to consent
• Surrogacy and legal parenthood – changes from 1 October 2013

• CE(06)08 - 30/11/2006

  HFEA Policy for the publication or withholding of centre data

• CE(06)07 - 25/09/2006

  HFEA consultation on annual fees for centres licensed under the European Tissue and Cells Directive

• CE(06)06 - 15/09/2006

  Import and export of gametes and embryos: future arrangements and transitional period

• CE(06)05 - 31/08/2006

  Consent forms

• CE(06)04 - 26/07/2006

  Licensing of research - Revised progress reports and initial and renewal application forms

• CE(06)03 - 27/07/2006

  Update on Special Directions to Import Gametes and Embryos

• CE(06)02 - 20/07/2006

  HFEA consultation on application fees for licensing under the European Tissue and Cells Directive

• CE(06)01 - 28/04/2006

  HFEA Standards for Assisted Conception Centres

• CE(05)02 - 30/06/2005

  HFEA Guide to lnfertility and Directory of Clinics

• CE(05)01 - 23/02/2005

  To clarify that research centres are expected to adhere by the requirements outlined in parts 2.23 to 2.26 of the Code of Practice (6th edition)

• DCE(05)01 - 01/06/2005

  Reporting of adverse incidents in research centres

• CE(02)01 - 04/10/2002

  Selecting donated gametes for treatment.

• CE 1 October 2002 - 01/10/2002

  HFEA Fee Increase

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Page last updated: 24 August 2012

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