Individual Case Safety Report (ICSR) Services

Individual Case Safety Report (ICSR) standards vary with every product type. With the continuous increase in ADR cases from various sources resulting from research and development, there is always a need to align with improved ICSR case processing standards and regulations. In such scenarios, to comply with the Health Authority (HA) requirements, organizations might opt for specialized ICSR pharmacovigilance services under the adverse event reporting system.

As an end-to-end pharmacovigilance service provider, Pharma Wizard’s ICSR pharmacovigilance services include product safety aspects from the developmental phase to the post-approval phase. 

Pharma Wizard also assists organizations in handling all types of medicinal product/device cases and various report types, including but not limited to spontaneous, literature, interventional & non-interventional clinical trial, pregnancy, legal, Over the Counter (OTC) products, end-of-study unblinding, compassionate supply, and named patient use reports.