Deconstructing the Drug Development Process: A Clarion Call for Improving R&D Efficiency
Brace for Impact: The Looming Data Submission Implosion
StatOps: Tackling Inefficiency to Accelerate Cycle Time
WHY BOOK YOUR V.I.P SEAT NOW?
You will be amongst 10-15 Industry thought leaders from a mix of large Pharmaceutical Institutions ensuring you are given ample opportunity to raise questions and contribute from a strategic perspective. You can wine, dine and network with industry leaders who face common challenges in 60-minute roundtable discussions that enable you to share ideas and lessons learned. The dinner will be facilitated by expert moderators, these sessions provide a valuable dialogue with peers on current challenges and topical issues. There is no media, marketing or press, just pure and honest discussion to help solve your key strategic challenges for the next 3-9 months.
Meet the Facilitators
The Dinner will be lead by our expert facilitators
Chris ConnorDirector of Product Management and Solution Strategy MaxisIT
Kenneth I. KaitinProfessor of Medicine and Senior Fellow Tufts University School of Medicine and Tufts Center for the Study of Drug Development
More about MaxisIT
MaxisIT simplifies clinical development with an easy-to-use integrated technology platform that automates repetitive tasks,streamlines workflows, improves data quality, and delivers role-based data in near-real-time to all team members. Our Clinical Trial Oversight System also includes a DMW (Data Management Workbench) and SCE (Statistical Computing Environment) with 50+ data visualization dashboards, access to clinical and operational repositories, AI-enabled clinical data mapping, validated data ingestion and refresh – all connected via a standards-based clinical metadata repository. Our cloud-based platform and services allow businesses to focus on clinical R&D, stay agile, make better decisions, uncover issues faster, and ultimately improve the quality of clinical trials while improving the patient experience.