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Page 1 of 3
Date Title
24/05/2013 Tissue establishment annual reports
20/12/2012 Serious adverse event (SAE) / Serious adverse reaction (SAR) report form - Organs
18/06/2008 Reporting Serious Adverse Reactions (SARs) and Serious Adverse Events (SAEs) associated with Human Tissues
04/01/2013 Regulatory requirements for the procurement, in the Republic of Ireland, of Human Tissues and Cells intended for human application
07/04/2011 Notification for invalidation fee
01/08/2006 Minimum Requirements for Blood Bank Compliance with Article 14 (Traceability) and Article 15 (Notification of Serious Adverse Reactions and Events) of EU Directive 2002/98/EC
19/02/2008 Irish Medicines Board Newsletter No 28 September - December 2007
03/02/2004 Irish Medicines Board Newsletter Issue No. 16
16/01/2007 IMB Newsletter, Issue No. 25 August - December 2006
01/10/1999 IMB Newsletter Winter 1999
01/06/1999 IMB Newsletter Summer 1999
01/06/2000 IMB Newsletter Spring Summer 2000
01/11/2002 IMB Newsletter No.12 - May - August 2002
08/10/2001 IMB Newsletter No. 9 - April - August 2001
16/07/2001 IMB Newsletter No. 8 - October 2000 - March 2001
01/11/2000 IMB Newsletter No. 7 - April - Sept 2000
09/10/2003 IMB Newsletter No. 15 - May - Aug 2003
28/05/2003 IMB Newsletter No. 14 - January - May 2003
01/10/2002 IMB Newsletter No. 13 - September - December 2002
01/02/2001 IMB Newsletter No. 10 - September - December 2001
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Date Printed: 19 June 2013

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