The medicines and medical devices regulatory landscape in Northern Ireland
Join us for a half-day session where MHRA experts will provide the latest updates on medicines and medical devices regulations.
The afternoon will begin with a networking lunch at 12:00, followed by an introduction from Diana Githwe, Partnerships Policy and NI Engagement Lead (MHRA), at 12:45. Attendees will then have the opportunity to drop into one or more of four focused workshops, each led by MHRA specialists and designed to support you in your current area of work.
The four workshops are:
12:45-12:50 : Regulation of Clinical Trials of Investigational Medicinal Products (CTIMPs) – Crina Cacou, Head of CIT Operations
12:50-13:25: MHRA Process for Managing Applications for Clinical Investigations – Mark Grumbridge, Head of Clinical Investigations
14:25-14:55: Parallel Review Applications – Mark Grumbridge, Head of Clinical Investigations
15:00-15:45: Flexibilities on Setting Up Clinical Trials Involving Companion Diagnostics in Northern Ireland – Louise Blakemore, Diagnostics Assessor
The workshops will end at 15:50, which will be followed by closing remarks from Christiana Ogunbote, Head of National Partnerships (MHRA).
