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Postmarket surveillance: a review on key aspects and measures on the effective functioning in the context of the United Kingdom and Canada
Regulatory approvals for the marketing of medicinal products authorize medical practitioners to prescribe drugs to a group of patients that are defined within the license of the medicinal product. However, such prescriptions are carried out in a controlled manner. Prior to being approved, the medici...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
SAGE Publications
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661791/ https://www.ncbi.nlm.nih.gov/pubmed/31384423 http://dx.doi.org/10.1177/2042098619865413 |