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Leveton and others published "HIV and the Blood Supply: An Analysis of Crisis Decisionmaking".

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Dr Edward Shanbrom, who worked as a vice-president of medical and scientific affairs at Hyland, developed the first commercially marketed freeze-dried Factor 8 concentrate. However his suggestions only attracted minimal support in the 1970s and very early 1980s.

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In Parliament, Baroness Jean Trumpington made clear that NHS products derived from screened plasma would become available for distribution during August 1986 throughout the UK.

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A surveillance of previously untreated patients for possible virus transmission by BPL Factor 8 and Factor 9 Concentrates, 8Y and 9A, was carried out in September 1986.

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BPL's work on heat treatment - regarding Factor 9 - only really started in 1982.

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The concern that heated Factor 9 concentrates might cause thrombosis was one that had to be resolved before its product could be issued. As a result experiments in dogs were conducted prior to clinical trial in humans.

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Hyland had a research project aimed at eliminating NANBH in factor concentrates that was being hindered by a lack of manpower and adequate funding.

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In February 1979 Hyland learnt of Behringwerke beginning clinical trials in 1978 in Germany on "Factor VIII Behringwerke" via a report to their head office, later confirmed by another Hyland employee.

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Hyland had heard that the clinical trials of the Behringwerke product were almost complete and had promising results.

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Hyland listed hepatitis risk removal from Hemofil as a project proposal. It noted that the removal of the risk of hepatitis transmission by Hemofil was needed in order to allow sales of the project excess inventories at the highest possible selling price.

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A letter from Dr Sternberg noted that by 1980 the research and development department of Cutter had made a strategic commitment that all new plasma products would be pasteurised.

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"The Advocate" newspaper article noted that in the early 1980s drug companies turned down a chemical process that could have prevented the infection of thousands of people with haemophilia with AIDS.

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An internal correspondence from Dr William Terry noted that due to contractual arrangements Dr Prince was precluded from publishing, without their approval, data from experiments supported by RHCG.

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The minutes of the Plasma Executive Committee noted that centres where unscreened donor product may have been delivered would not be contacted until the situation was clear.

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A memo from Dr Harris to Mr Christie outlined that on 27 February 1986 Dr Harris visited Dr Whitmore at Lewisham Hospital and followed up the history of two people with haemophilia who had seroconverted to HTLV-3 positive following treatment with heat-treated Factorate.

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A memo from Dr Harris to Mr Christie outlined that he was now obliged to report Dr Whitmore's seroconverted patient to Dr Rotblatt as Dr Whitmore had confirmed that the patient remained HTLV-3 positive following receipt of heat-treated Factorate.

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Christopher Bishop wanted to prepare a "defence" document designed to restore confidence in Armour's heat treatment process and stop further deterioration in sales.

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Cutter's product, Koate HT, had been available since November 1984.

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An internal sales report to Cutter showed a determination to continue to try to sell heat-treated products.

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Some treatment centres continued to use un-heat-treated product due to cost pressures.

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