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How connected devices are making trials more patient centric.
Released By IQVIA
Insights and best practices for a new era of drug development
Addressing increasing complexity, cost of drug development, and navigating regulatory compliance.
By: Kristin Brooks
How can early decisions in cell and gene therapy clinical development impact downstream progress toward commercialization and patient access?
By: Dr. Diego Correa, Erin Finot
Spreen previously served as Chief Commercial Officer at IQVIA.
By: Charlie Sternberg
Isaac Batley offers 35 years of leadership experience working in healthcare communications within the pharmaceutical sector.
Modi brings extensive experience from the life sciences industry, having held leadership roles at both IQVIA and GSK.
Stafford offers more than 35 years of industry experience.
Ratliff succeeds Ludo Reynders, who will be retiring and will become an advisor to the company and remain a board member.
Research & Development Solutions revenue up 7% to $2.1 billion.
Regulatory agencies are adapting to the digital age by implementing processes and documentation enabled by modern technology.
By: Rama Mohan
Brown is currently UBC’s chief operating officer with more than 20 years of senior management experience.
Robbie has more than 25 years of experience with biomarker assay technologies, including 20 years of experience in scientific leadership positions.
New workflow tool delivers enhanced AI-driven customer engagement.
Total baseline value for Emergent is approximately $90 million USD, further expanding the collaboration between the companies, which began in February 2021.
Released By Emergent Bioservices
A retrospective look at how the industry aimed to maintain trial continuity—what worked well as is, what needed improvements, and what's here to stay.
By: Dr. Cynthia
Lessons learned from operationalizing hybrid DCT solutions across the globe.
By: Ronan brown
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