For clinic staff and other professionals

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Helping you ensure your fertility or research clinic is following current regulations and guidance.

Code for Clinics

8th Code of Practice

The HFEA Code of Practice is intended to help and encourage licensed centres to understand and comply with their legal requirements.

It also gives guidance on how centres are expected to go about meeting those requirements.

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Guidance

Directions: Directions are essentially rules that clinics need to follow. They have been updated to reflect changes in the Human Fertilisation and Embryology Act 2008 and in HFEA policy.   

Chair's letters: Notifications to licensed centres of changes to HFEA policy.

Chief Executive's letters: CE letters provide relevant information about developments at the HFEA and notify licensed clinics of changes to HFEA operating procedures.

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Forms to use in your clinic

Consent forms: Record patient consent to various aspects of fertility treatment.

Patients and donors registration forms: Record the registration of fertility treatment patients, and their partner, at your clinic. Includes welfare of the child form.

Clinic operation forms: inlcudes - Confidential declaration form, Person Responsible or Nominal Licensee form, Import and export of gametes and embryo forms and ICSI practitioner forms.

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Inspecting your clinic

Inspection reports - treatment and storage: Read the results of your clinic’s inspection. The latest reports are posted once they have been reviewed and approved by the HFEA’s Licence Committee.

Inspection reports - research: These reports examine a centre’s application to undertake a particular research project. Read the results of your research centre’s latest research inspection report.

Prepare for your inspection: Read our guide that explains what Persons Responsible and their staff can expect before, during and after an inspection.

...more about our inspections

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Guide to licence applications and inspections

The guide to licence applications and inspections will take you through the process of applying for your first licence, renewing an existing one and preparing for your inspection. 

You can also find out how to make variations to a licence you may already hold.

Getting a licence can be an involved and lengthy process - make sure you are prepared before starting the application process. 

...read the guide to licence applications and inspections

Quality Indicators

You asked for help in establishing quality objectives

We asked the sector and some of their suggestions can be downloaded below.

These are not mandatory requirements - just examples for your guidance: 

Further information on quality indicators, and how they can be implemented, is available from:

Login to the Clinic portal

Login to update your clinic's details, apply for treatment, storage and research licences, read incident alerts, complete the SAQ and Special Directions.

Clinic portal login

Forgot your login details? Contact us for help portalsupport@hfea.gov.uk

PR Entry Programme - PREP

The law requires licensable activity to take place only under the supervision of a Person Responsible.

An individual can be appointed as the PR only with the approval of the HFEA. That person must complete the Person Responsible Entry Programme (PREP) assessment before the HFEA can consider whether or not to approve them.