Event Date: 22/06/2012 01:00
The Irish Medicines Board is pleased to announce that we will hold a seminar on Tuesday 19th June 2012 in the Irish Medicines Board, Kevin O'Malley House, Earlsfort Terrace, Earlsfort Centre Dublin 2.
This meeting will address the requirements for medical practitioners conducting clinical trials of medicines as investigators or sponsors.
Aims of the Seminar
The information seminiar will address the following topics:
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the application process for clinical trials;
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relevant legislation and guidelines;
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substantial amendments;
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end-of-trial declarations and reports;
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development safety update reports (DSURs);
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urgent safety restrictions
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adverse reaction reporting;
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responsibilities for sponsors and investigators; and
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findings from Good Clinical Practice (GCP) inspections.
Presentations given on the day are available to view/download at the links below:
Who Should Attend
This seminar will be of interest to medical practitioners conducting clinical trials as sponsors (academic trials) or as investigators (commercial or academic trials). Site staff are welcome to attend.
Fee & Venue Details
Date: 19th June 2012
Time: 17.00 - 19.00 (Registration will take place at 16.30)
Venue: Health Products Regulatory Authority
Kevin O'Malley House
Earlsfort Terrace
Earlsfort Centre
Dublin 2
Fee: There is no fee to attend this event.
Light refreshments will be provided