Drug safety regulations
Drug safety regulations incorporates several mutually reinforcing activities all geared toward promoting and protective public health. It demands the application of sound medical, scientific and technical data and skills that will operates within a legal framework. These activities vary from country to country in scope and implementation. The Medicines and Healthcare products Regulatory Agency is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe. The aim of the Pharmacovigilance and Pharmacoepidemiology Journal is to publish high quality research in the discipline of Pharmacovigilance by providing encouragement for editors, reviewers, authors, and readers to have an uninterrupted scientific communication.
PDF
