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Earlier availability of virally inactivated concentrates would have made the biggest difference.

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Some Factor 8 product had been recalled, but this was probably a batch recall rather than a general recall.

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Dr Milton Mozen, the director of biochemical research and development at Cutter, emphasised in his evidence to the Institute of Medicine in the US that a heat treatment process is successful as applied by one manufacturer, it does not follow that this process would be applicable to the unique products of the other manufacturer.

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Dr Peter Fernandes stated that similar stabilisers to those which worked with the globulin could work with antihemophilic factor.

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Clive Collins stated that ,"Given the specialised medical nature of the seroconversion problem it was appropriate that my Medical Department colleagues dealt directly with the DHSS Medical staff."

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Dr Shanbrom had suggested to the executives that they should no longer take plasma from hepatitis hotspots such as downtown Los Angeles and from prisons because of the risks.

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J K Smith, Lowell Winkelman and P A Feldman reported the interim results that severe heating had been more effective in preventing transmission of non-A non-B Hepatitis than the milder heating given to at least two US commercial products.

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A clinical trial of 8Y was reported to be at a stage where several patients had safely passed the point at which first evidence of non-A non-B Hepatitis transmission would have been expected.

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Milt Mozen visited SNBTS PFC and discussed the issue of hepatitis with Jim Smith.

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Dr Peter Foster was shocked when Dr John Cash told him that the German company Behringwerke had announced at a symposium in Bonn that it was pasteurising Factor 8, as he had thought heat could not be used to inactivate virus in factor products.

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Dr John Cash established the SNBTS Coagulation Factor Study Group.

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PFC produced 11 pilot batches of "ZHT" and tested their clinical validity in late 1983.

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PFC and SNBTS prioritised dry heat treatment over pasteurisation after the the data presented at Groningen showed that it could inactivate HTLV-3.

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PFC heat treated its existing 12-month stock of Factor 8 batches manufactured as early as October 1983.

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PFC heat treated products for 24 hours (extended from 2 hours).

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PFC experienced issues with the freeze drying process in relation to the production of Z8.

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Clinical trials of Z8 were delayed due to a question about compensation to patients who might be harmed during the trials raised by Prof Ludlam, supported by all of Scotland's haemophilia doctors.

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Dr Peter Foster was head of the R&D Department of the SNBTS PFC.

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Dr Peter Foster was a biochemist at PFC.

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A H Woodhead wrote to all Blood Transfusion Service directors about a batch of Factorate recalled by Armour Pharmaceuticals.

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