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The Inquiry's interim report highlighted the importance of ensuring Hepatitis B sufferers had been supported in any compensation scheme that might occur.

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Compensation could not be given for those infected with Hepatitis C as a result of a donation that was given after 1 September 1991. No case would be reviewed that did not meet this cut off point.

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Long-lasting effects of Hepatitis C were not fully considered by the funds and compensation schemes as it was difficult to identify symptoms of the disease before it was formally diagnosed.

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John Dillon noted that according to the evidence of the Expert Group on Hepatitis, 20% of Hepatitis B infections would clear spontaneously.

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Unsuccessful applicants to the Skipton Fund were ignorant of the detail of reasoning that led to the rejection of their claims. Nicholas Fish noted that those who had asked for a copy of letters and reports relating to their decision would have been given one.

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Some applicants who admitted to intranasal or oral drug consumption, but not to injection, were denied on the basis of intravenous drug use, even though their medical records contained no reference to any such use.

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Mark Mildred was told by Nicholas Fish when he began working for the Skipton Panel and asked what sort of decision was wanted, to provide "A letter, keeping it as brief and simple as you can."

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Mark Mildred was not initially given, nor did he ask for, a copy of the Agency Agreement under which the Skipton Fund operated under the Department of Health.

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William Vineall stated in his evidence: "we think the testing regime that was established, I think in about 1972, for hepatitis B was sufficient to ensure that people with hepatitis B wouldn't be, you know, subject to the risk of infected blood, and that's why it's never been part of any scheme".

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Dame Marcela Contreras advised that where GP records for the time were available, they may have included discharge letters which may have referred to transfusions, but equally may not.

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Dr Patricia Hewitt suggested that though records should have been made to show that a transfusion had been given, and identifying numbers of the transfused units recorded, practice about this was often casual, and records were often not retained for the length of time necessary to help show some years later that a transfusion had taken place.

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The Secretary of State for Health, Alan Milburn, was opposed to a compensation scheme or payments, largely on the basis that they would set a precedent, especially since his view was that no fault had been demonstrated.

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Susan Deacon ordered an inquiry into whether people with haemophilia in Scotland had been exposed to unnecessary risk of Hepatitis C through infected blood products in the mid 1980s.

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The Health and Community Care Committee of the Scottish Parliament considered the Haemophilia Society petition calling for a public inquiry, and a second petition from a person who had contracted Hepatitis C as a result of a blood transfusion during a routine operation in 1989.

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The Health and Community Care Committee called Susan Deacon to give evidence on 25 October 2000.

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Alan Milburn told the Treasury that the legal advice for the Government was that there was a very limited chance of success following the recommendations in the judgment of the High Court (in England) in "A and Others v the National Blood Authority" and the decision should not be appealed.

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The Skipton Appeals Panel met quarterly. A guidance note was provided to applicants which clarified that they could provide evidence of a transfusion.

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In "A and Others v the National Blood Authority" Mr Justice Burton concluded that routine screening ought to have been introduced by 1 March 1990, and surrogate testing should have been in place by March 1988.

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An amendment to the Skipton Fund occurred in 2016 which made specific clauses applicable to each UK nation.

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The Scottish Executive announced that an expert group, to be chaired by a Court of Session Judge, Lord Donald Ross, was to be set up to look at the pros and cons of a system of financial and other support for those harmed by health service treatment where the NHS was not at fault.

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