Clinical Trial Supply Nordics

After the challenges of 2020 with the Covid-19 pandemic, this is the unmissable event that the pharmaceutical, biotechnology, and medical device communities need to come together and discuss strategies for operational success in clinical trials.

With all the latest content, and a big focus on the latest regulations and technology, the conference will offer an unparalleled opportunity to hear in-depth talks from the likes of the Danish Medicines Agency, LEO Pharma, and TÜV SÜD, as well as C-level and senior experts from the Nordic region.

The event will feature talks and interactive sessions on the hottest topics of the year including:

• The future of EU Clinical Trial Regulation: opportunities to streamline multinational trial approval – Lene Grejs Petersen, Senior Advisor, Danish Medicines Agency
• A panel discussion on regulations in decentralised trials including both the Swedish and Danish Medicines Agencies
• The Notified Body perspective: the future of drug-device combinations with the upcoming Medical Device Regulation (MDR) – Dr. Christiana Hofmann, TÜV SÜD

Henrik Schlieker and Alan Lahaise from PCI will be at booth 9 and available to discuss your global clinical supply chain requirements

For more information or to register for this event, please see the event website