Andrea Charles | 06/14/2013
The FDA Final Rule on UDIs (unique device identifiers) for medical devices is expected to be published in early August. In May the EU Commission announced their intention to take an internationally harmonised approach and follow the FDA's decision over here in Europe. In this exclusive interview Inge Ørnhøj, Senior Process Improvement Manager, Supply Chain Process Improvement at Coloplast A/S, speaks to Andrea Charles from Pharma IQ, about the impact...
To continue reading this story Click Here
Upcoming Events
GenAI Life Science & Health 2025
September 1 - 3, 2025
Berlin, Germany
Register Now |
View Agenda |
Learn More
DigIT Pharma AI Commercial Excellence & Health 2025
September 1 - 3, 2025
Palace Hotel Berlin, Germany
Register Now |
View Agenda |
Learn More