ICSR Management
ICSR Management:
The management of individual suspected adverse reactions and events is the basis of Pharmacovigilance and safety monitoring. We help you in the correct collection, processing, assessment, submission and follow-up of activities and reconciliations in all the following fields:
Clinical trials
Complete management and assessment of SAE / SUSARs
Post Authorisation
Complete management and assessment of ICSRs
Medical Devices Vigilance
Adverse Incident Management
Cosmetovigilance
Adverse Event Management
Literature searches
On a local and international level, including MLM searches.
We can also support you in the management of medical information queries related to the safety of your products.
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