Minutes of the Eighteenth Annual General Meeting of the UK Haemophilia Centre Doctors Organisation. Consent and data protection discussed following a review of the National Haemophilia Database by Professor Charles Hay. Noted that the main database functioned on implied consent with an opt out. Hay recommends that mixed-use of patient data requires consent, and this should be done face-to-face. Launch of Public Inquiry discussed, and the Haemophilia Society is to recommend that the inquiry is directed at the decisions made by the DoH rather than individual clinicians. Appendix 1 attached showing list of attendees.