Results for 'organizational changes'



Comparative study on anticancer drug access times between FDA, EMA and the French temporary authorisation for use program over 13 years
Apr 7th • 12 mins read

Virtual Clinical Trials in Oncology-Overview, Challenges, Policy Considerations, and Future Directions
Apr 8th • 4 mins read

Advances in basic research in oncology in 2020: Bridging basic science and clinical care
Mar 24th • 1 min read

Assessment of Coverage in England of Cancer Drugs Qualifying for US Food and Drug Administration Accelerated Approval
Feb 22nd • 10 mins read

The regulatory landscape of precision oncology laboratory medicine in the United States - Perspective on the past 5 years and considerations for future regulation
May 22nd • 8 mins read

Access to Novel Drugs for Non-Small Cell Lung Cancer in Central and Southeastern Europe: A Central European Cooperative Oncology Group Analysis
Nov 24th • 10 mins read


Patient involvement: A must-have in medicine development, but is it being overlooked in a cost-constrained environment?
May 9th • 5 mins read


Medical affairs: The power behind redefining commercialization
Aug 2nd • 3 mins read


Empowering people to drive medical affairs performance with AI
Aug 14th • 5 mins read

Are the chronological age cutoffs used in clinical oncology guidelines biologically meaningful?
Dec 1st • 4 mins read

Report from American Society of Clinical Oncology Symposium 2020 and American Society of Clinical Oncology Gastrointestinal Cancer Symposium 2021
Aug 4th • 13 mins read

Regulatory and clinical consequences of negative confirmatory trials of accelerated approval cancer drugs: retrospective observational study
Aug 4th • 12 mins read

Overview of Oncology and Hematology Drug Approvals at US Food and Drug Administration Between 2008 and 2016
Aug 4th • 15 mins read

Cancer research in the United States: A critical review of current status and proposal for alternative models
May 14th • 10 mins read

The FDA Oncology Center of Excellence and Precision Medicine
Nov 6th • 3 mins read