Data is the key to improving Patient Safety across the globe.
Identification of Medicinal Products (IDMP) is a suite of five standards developed within the International Organisation for Standardisation to facilitate the unique identification of medicinal products in the context of pharmacovigilance and the safety of medications throughout the world.
This new set of data standards will revolutionise the manufacturing, distribution, and regulation of medicinal products globally. It establishes data standardisation throughout the entire product lifecycle, encompassing development, investigational products, evaluation, and authorised products.
IDMP aims to enhance the reliable exchange of medicinal product information, promoting interoperability across regulatory and healthcare communities worldwide. This fosters accurate analysis and unambiguous communication across jurisdictions.