The European Medicines Agency (EMA) has updated its identification of medicinal products (IDMP) implementation guide, providing additional details on topics including the basis for medicinal product ...

The European Medicines Agency (EMA) has published a guide to implementing IDMP data standards that will be ”a game changer” for the life sciences sector. Remco Munnik, who has been working with the EU ...

The recent publication of the European Medicines Agency’s (EMA) latest version of its EU IDMP (Identification of Medicinal Products) Implementation Guide is something of a landmark for the industry.

The European Medicines Agency (EMA) has recently published the second version of its EU IDMP Implementation Guide, and it is a landmark regulation for software vendors and pharma companies alike. This ...

Substantial investment has gone into the preparations for the EU’s implementation of the ISO IDMP (identification of medicinal products) standards, which must not be compromised in 2020 - whatever the ...

The European Medicines Agency (EMA) has announced it is putting together a task force to oversee the implementation of new standards for identifying drugs. The goal of the task force will be to ...

Many pharmaceutical companies are sceptical about IDMP despite the business benefits and its contribution to patient safety. The European Union is aiming to play a big role in the creation of a global ...

As Europe moves closer to implementation of ISO IDMP standards, the bio/pharma industry is accelerating efforts to manage its data and documents more effectively. As the world becomes increasingly ...