In the News
April 30, 2026
Parexel Acquires Vitrana to Expand AI-Enabled Patient Safety and Pharmacovigilance Technology
April 27, 2026
S.Biomedics Selects Parexel as Contract Research Organization (CRO) to Accelerate U.S. Development of TED-A9 for Parkinson’s Disease and Japanese Market Entry
April 22, 2026
After Contributing 30% of Global Innovation Assets, What’s Next for China’s Innovative Drug Industry?
April 20, 2026
How Sponsors Should Be Structuring Development Plans Around the Plausible Mechanism Framework Right Now
April 17, 2026
The Evidentiary Risks of Natural History Data and How to Approach External Control Comparability
April 16, 2026
Where Master Protocols Are Most Vulnerable Under the Plausible Mechanism Framework
April 15, 2026
How Regulators Assess Substantial Evidence When Trial Populations Are Too Small for Traditional Designs
April 14, 2026
How FDA's Plausible Mechanism Framework Changes the Path to Approval for Individualized Therapies
March 10, 2026
Four strategies for executing complex, international phase 3 breast cancer trials
March 4, 2026
Parexel Execs On Trials In War Zones, Biotech 'Green Shoots', China Action and DCT Rework
March 2, 2026
Scientifically rigorous and resolutely empathetic: how pharmacovigilance programmes can elevate the patient voice
February 27, 2026
Equitable Care, Accelerated Timelines: Expanding Global Access to Rare Disease Research
February 26, 2026
Finding Hope for FRRS1L Selects Parexel for Regulatory and Investigational New Drug (IND) Support with US Food and Drug Administration (FDA)
February 3, 2026
Meeting Halfway: Co-Developing Frameworks for Seamless FSO to FSP Transitions
February 2, 2026
Industry calls Union Budget 2026 a defining moment for India's biopharma future
January 21, 2026
India at a jumping-off point in terms of commitment to global clinical studies