Clinical Trial Supply 2020 – A Virtual Experience

Arena International Announces the Virtual Experience of Clinical Trial Supply Conference Series

London – Arena International announced today that the Clinical Trial Supply Conference (https://arena-international.com/ctsvirtual/) will be held as a Virtual Experience on Tuesday, 12 May, 2020, providing the immersive online platform that the pharma supply industry needs to come together and tackle pressing supply challenges amid the crisis. 2020’s Virtual edition will continue to bring engaging networking opportunities and cutting-edge content in pharma supply chain direct to your screen.

The landscape of clinical trials in the global market is becoming increasingly complex. Pharmaceutical companies running clinical studies must overcome many issues, having to work within a budget, stick to timelines, handle vast amounts of data, and often operate overseas. These trials are usually conducted on a large-scale with thousands of patients at multiple sites, which brings significant logistical and operational challenges.

This virtual edition will offer case studies and insight into how to effectively manage operational issues across the clinical trial supply chain. Attendees can stream live and prerecorded presentations from the FDA, senior executives from the likes of Portola Pharmaceuticals, and Gilead and delve into the hottest topics of year including Big Data & AI. Connecting with other industry leaders will also made possible with the new Meet the Experts discussion session and via the platform’s live chat and video chat features– equipping attendees with the ability to reach their peers and colleagues globally.

A preview of the key sessions:

Maturing Global Trade Compliance (GTC) To Add Value in The Growth of a Biotech. Patrick Pillsbury, Associate Director, Logistics and Global Trade Compliance, Portola Pharmaceuticals.

Unlocking the Potential for Big Data and Artificial Intelligence. Prasun J Mishra, Chief Executive Officer, Agility Pharmaceuticals.

An Overview of FDA’s Office of Pharmaceutical Quality Operations and How to Ensure the Timely Importation of Drug Products. Lance De Souza, Compliance Officer, Division of Pharmaceutical Quality Operations, FDA.

Outsourcing in Clinical Trials 2020 - A Virtual Experience

Arena International Announces the Leading Outsourcing in Clinical Trials Conference as a Virtual Experience

London – Arena International announced today that the Outsourcing in Clinical Trials Conference (https://arena-international.com/octvirtual/) will be held as a Virtual Experience on Wednesday, 27 May 2020, providing the ideal platform to talk about the impact of crisis on the pharma industry and discovering best approaches to CRO, Sponsor and Patient relationships. 2020’s Virtual edition will continue to bring engaging networking opportunities and cutting-edge content specifically for Outsourcing in Clinical Trials direct to your screen.

Outsourcing in Clinical Trials is the ideal platform to talk about the impact of crisis on the pharma industry and to further demonstrate the need adapt and learn in trying times for more efficient practices and improved CRO, Sponsor and Patient relationships. Attendees will be able explore and learn how the market is coping with changes in regulations, opportunities through adaptive approaches and methods to run successful clinical trials.

This virtual edition will offer case studies and insight into how to effectively and efficiently improve CRO, Sponsor and Patient relationships. Attendees can stream live and prerecorded presentations from top tier speakers on topics surrounding relationship building between CROs and trial sponsors, the impact of Medical Device Regulation (MDR) and ICH E8 (R1) compliant, among others.   Connecting with other industry leaders will also made possible and via the platform’s live chat and video chat features– equipping attendees with the ability to reach their peers and colleagues globally.

A preview of the key sessions:

Strategies for Efficient Conflict Resolution Between Trial Sponsors and CROs. John Shillingford, Director of Clinical Research, Afon Technologies Ltd.

Case Study: Can Choosing an Adaptive Approach Lead to Increased Efficiency in a Clinical Trial? David Wright, Head of Clinical Operations Western Europe, Janssen Inc.

Impact of the Medical Device Regulation on Device Approvals. Andrew Thompson, Director of Therapy Research & Analysis, Medical Devices, GlobalData.

AI in Healthcare Online Masterclass

AI is getting increasingly sophisticated at doing what humans do, but more efficiently, more quickly and at a lower cost. The potential of both AI and robotics in healthcare is vast. Just like in our everyday lives, AI and robotics are increasingly becoming a part of our healthcare ecosystem.

The masterclass will enable the participants to learn how to leverage AI for providing better patient experience, optimise operational efficiency and improve business performance.