‘ICSR’ refers to Individual Case Safety Reports which must be compiled for each instance of a suspected or confirmed adverse event and each reception of a report about one to the Competent Authority (CA) of the Member State.
Remaining compliant throughout all the changes to EU legislation can be a challenging endeavour for any company. This is particularly the case with Expedited Reporting – one of the pillars of all EU pharmacovigilance work.
Companies are required to prepare detailed periodic safety update reports on all their products that have marketing authorisation in the EU.
Why Are Correct Screening Procedures So Important?
Business-Critical Responses – Your Processing of Safety Signals
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