Even now, after a decade of run-up, pharma’s readiness to implement and harness ISO IDMP standards still varies wildly, as does companies’ relative maturity in supporting FAIR data principles, geared ...

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.

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 ...

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 ...

Pharm Exec speaks to Andrew Marr about the implications of the European Union's new IDMP (Identification of Medicinal Products) regulations for the pharma industry. At this year’s AMPLEXOR “Be The ...

Up to now, the pharma industry’s advances in implementing ISO IDMP product data standards have been patchy. New research has looked more closely at companies’ IDMP readiness, as well as their progress ...

NORTH BETHESDA, MD – Regulators around the globe are making progress in implementing the Identification of Medicinal Products (IDMP) a global set of standards for identifying medicinal products. The ...

EMA’s SPOR implementation guide version two is expected to be published soon, starting the countdown for companies to ensure their data-based submissions are compliant. A revised series of standards ...