Patient safety data is a resource that doesn’t just stop coming in once your product gets approved. Sponsors are responsible for the safety of their products from the clinical trial stage through post market. This fact sheet from Worldwide Clinical Trials, entitled “Patient Safety, Sponsor Security,” discusses the components of an end-to-end pharmacovigilance program. In it, we outline the services Worldwide offers to help sponsors safeguard patient well-being and maintain regulatory compliance.
