In today’s ACT Brief, we examine three priorities for first-time APAC sponsors, how continuous glucose monitoring should be used in diabetes trials, and why FDA is requiring a new eye-related warning across GLP-1 medications.
|Articles|August 1, 2011
- Applied Clinical Trials-08-01-2011
- Volume 20
- Issue 8
Applied Clinical Trials Digital Edition - August 2011
CRO/SPONSOR : Clinical Contracting Efficiency Can Save Millions REGULATORY : Common Technical Document Development - A Partnership Approach Also in this issue : FDA Looks to Collaborate Overseas, EU Reviews, Clinical Trial Rules, Meaningful Web, Greater Trial Insight
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Applied Clinical Trials Digital Edition - August 2011, Supplementover 15 years ago
Change the CT Rules, but to What Precisely?over 15 years ago
EFGCP Advocates Change to Consent Processover 15 years ago
Digital Data, the Semantic Web, and Researchover 15 years ago
Business and News Update August 2011over 15 years ago
An Idea Whose Time Cameover 15 years ago
FDA Seeks New Approach to Global Challengesover 15 years ago
In Pursuit of Enlightenmentover 15 years ago
Clinical Contracting Efficiencyover 15 years ago
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In this video interview, James Cheong, senior vice president of Asia Pacific at Precision for Medicine, shares three priorities for first-time APAC sponsors: aligning with marketing authorization plans, selecting the right sites, and choosing a CRO with regional experience and KOL networks.
FDA and EMA expectations shape how sponsors use CGM in diabetes trials, from blinding and study-provisioned devices to data integrity and ePRO integration.
In today’s ACT Brief, we examine why APAC is attractive for global Phase III programs, how clinical research professionals can turn a failed pivotal trial into a redesigned success, and how FDA approved Sunharbo to reduce recurrent stroke risk.
A pivotal trial that missed its primary endpoint became the basis for a successful redesign after the team used the data to define the high-risk patients most likely to benefit, showing that setbacks can strengthen development when organizations interrogate the evidence rather than abandon it.
In this video interview, James Cheong, senior vice president of Asia Pacific at Precision for Medicine, outlines why faster recruitment, local data requirements for registration, and lower costs make APAC attractive for global Phase III programs.
In today’s ACT Brief, we examine how China’s trial startup timelines compare with those in the US and Europe, whether AI-drafted clinical study reports speed drug development, and how Bimzelx compared with Skyrizi in psoriatic arthritis.
AI can draft a CSR in minutes, but the report only reflects evidence that has already converged, so faster drafting shifts the bottleneck to upstream reconciliation, database-lock readiness, and human accountability rather than shortening the trial itself.
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