At the upcoming 12th Annual Outsourcing in Clinical Trials Nordics meeting, experts from the pharmaceutical, biotechnology and medical device industries, will gather in Copenhagen, Denmark, to provide an in-depth exploration of current trends and challenges in clinical trial operations, outsourcing, and management across two days.
The conference will commence with a talk on recent updates on the EU Clinical Trial Regulation (CTR) and Clinical Trial Information System (CTIS), providing key insights into the latest regulatory developments as well as learnings and tips on handling clinical trial submissions. One of the initial presentations will focus on the developments in technology and their impact on the transformation of the clinical research landscape.
A key theme of the conference will be the adoption of a more patient-centric approach and the reshaping of the clinical research landscape by leveraging data and incorporating cutting-edge technologies to improve trial results.
Another central focus of the event will be outsourcing strategies, featuring presentations on fostering strong vendor partnerships, optimising clinical trial protocols and governance structures as well as strengthening collaborations between sponsors and contract research organisations (CROs). The first day of the conference will end with an overview of the recent global trends in clinical trials and a focus on challenges in drug development for CNS disorders and rare diseases.
The second day of the conference will begin with a session on navigating the regulatory landscape for combination trials in the Asia-Pacific region, exploring advantages, challenges, country-specific differences, and updates specific to the APAC region. On this day, the sessions will delve into topics such as regulatory challenges, sustainability, and decentralised clinical trials (DCT).
A significant topic that will be addressed is sustainability in clinical trials, with a spotlight on the healthcare sector’s responsibility to implement best practices to minimise the environmental impact of trials.
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By GlobalDataJoachim Lovin, a DCT specialist at Novo Nordisk will present a sponsor case study and share insights on implementing decentralised trial elements post-Covid-19, highlighting the evolving state of DCTs, best practices, and tools for improved patient engagement. A fireside chat in the afternoon will explore risk management strategies in clinical trials, highlighting the significance of early feedback and oversight.
The conference will end with interactive roundtable discussions on clinical supply chain risks, effective engagement with CROs, and DCT trial designs, offering attendees the chance to engage directly with experts and peers to address critical industry challenges.
The conference is hosted by Arena International Events Group, a B2B events company owned by GlobalData, the parent company of Clinical Trials Arena and Pharmaceutical Technology.
A detailed agenda can be found here.
