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Date	Title
18/12/2008	Guide to Information held by The IMB
16/12/2008	Annual Report 2007
16/12/2008	Medical Devices Newsletter No. 24 - December 2008
08/12/2008	Acomplia (08 Dec)
02/12/2008	Prograf & Advagraf (tacrolimus)-Important Safety Information from Astellas Pharma following approval by the IMB
28/11/2008	Drug Substance Section of Dossiers - A Regulators view
19/11/2008	Lucentis (ranibizumab)-Important Safety Information from Novartis following approval by the IMB
07/11/2008	MabThera (rituximab)-Important Safety Information from Roche on rituximab and PML, following approval by the IMB
06/11/2008	Guide to Batch-Specific Requests for Human Medicines
05/11/2008	IMB Newsletter Issue No. 30 April - August 2008
04/11/2008	Raptiva (efalizumab)-Important Safety Information from Merck Serono on the association of efalizumab with PML
24/10/2008	Acomplia (rimonabant)-Important Safety Information from Sanofi Aventis concerning the suspension of Acomplia
03/10/2008	Perfalgan (paracetamol)-Important Safety Notice from Bristol-Myers Squibb regarding hepatic toxicity
30/09/2008	Arcoxia (etoricoxib)-Important Safety Information from Merck Sharp & Dohme following approval by the IMB
30/09/2008	Terms of reference and rules of procedure of the Clinical Trials Subcommittee
22/09/2008	Relistor (methylnaltrexone bromide)-Important Safety Information from Wyeth as approved by the IMB
17/09/2008	Drug Safety Newsletter 28th Edition
01/09/2008	Volume 9A of The Rules Governing Medicinal Products in the European Union
22/08/2008	Medical Devices Newsletter No. 23 - August 2008
20/08/2008	Adverse Reaction/Event Report Form Human Tissues and Cells