Development and rational use of standardised MedDRA queries (SMQs): retrieving adverse drug reactions with MedDRA, report of the CIOMS Working Group (2nd edition)
This publication aims to inform regulatory authorities, scientific institutions, pharmaceutical companies and other organizations or individuals involved in pharmaceutical and other medicinal product development, about the purpose and appropriate use of SMQs in safety surveillance activities.
Read More
This publication aims to inform regulatory authorities, scientific institutions, pharmaceutical companies and other organizations or individuals involved in pharmaceutical and other medicinal product development, about the purpose and appropriate use of SMQs in safety surveillance activities.
Read Less