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The collection of blood from closed prisons was stopped in England and Wales.

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The second NBTS leaflet on AIDS containing advice for blood donors was published.

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Long-term review (A Full Life; Not Just Existence) commissioned by the Macfarlane Trust suggested approaching the Department of Health for further funding.

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Dr Duncan Thomas inspected Hyland Laboratories in California noting a hepatitis hazard associated with the products as a result of the nature of the donors and the large plasma pools.

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CSM(B) recommended the grant of a product licence for Hemofil.

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CSM(B) recommended the grant of a product licence for Kryobulin.

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A product licence was granted for Profilate made by Abbott Laboratories Ltd.

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CSM(B) recommended a product license be granted for Factor 8.

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DHSS Divisional Management Group meeting considered criticisms made by the documentary World in Action: Blood Money of Travenol's production of Factor 8.

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Dr David Owen considered Armour's application to supply Factorate to haemophilia centres.

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CSM recommended the grant of a product licence for Koate.

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An application was made by Immuno to vary the product licence in respect of Kryobulin to allow European plasma to be sold in red packs and US plasma to be sold in cheaper blue packs.

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An application by Immuno to vary the product licence in respect of Kryobulin to allow European plasma to be sold in red packs and US plasma to be sold in cheaper blue packs was approved.

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The Department of Health and Social Security informed Immuno approval had been granted to vary the product licence in respect of Kryobulin to allow European plasma in be sold in red packs and US plasma to be sold in cheaper blue packs.

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Licences for heat-treated Hemofil and Factorate were refused.

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FDA recommendation of steps including avoiding use of high risk plasma in US blood products was published.

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Paper from Dr Spence Galbraith recommended suspending importation of US blood products.

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The CSM endorsed the recommendation by the CSM(B) not to recommend action to stop continued importation of commercial concentrates.

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CSM(B) decided not to recommend action to stop continued importation of commercial concentrates.

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It was confirmed that import of factor products made from higher risk pre-March plasma would continue.

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