Access to Adverse Reporting

CiPharma clients and network members are provided access training for our “Rapid Events” adverse reporting solution which enables automated, timely and accurate updating of the FDA MedWatch scheme. The system is designed to effectively manage and address undesirable experiences or adverse events associated with the use of any medical product.

We undertake initiatives to educate and support grassroots Healthcare professionals, consumers and patients. Our corporate citizenship program serves to ensure that no affected persons are disadvantaged in their ability to report adverse events. Inline with this goal CiPharma proactively seek and support subjects, supporting access to regulatory reporting channels and processes.