Wells Fargo and Pfizer CEOs warn that China is surpassing the U.S. in innovation, citing faster regulatory approvals and more supportive government policies.

Speaking at a conference, they noted China's streamlined processes allow new products and treatments to reach market significantly quicker than in America.

Wells Fargo's CEO pointed to China's rapid adoption of digital payments and fintech innovations, while Pfizer's chief highlighted that some drug approvals now happen faster in China than in the U.S., reversing the historical pattern. Both executives emphasized that excessive U.S. regulations and bureaucratic delays are creating competitive disadvantages.

They called for regulatory reform to help American companies maintain their innovative edge, warning that the current environment pushes investment and development toward countries with more efficient approval systems.

The comments reflect growing corporate concern about America's ability to lead in key technology and healthcare sectors amid increasingly complex compliance requirements. https://www.cnbc.com/2025/10/15/wells-fargo-pfizer-ceos-china-innovation.html #Innovation #China #USA #Regulation #Pharma #Fintech #Healthcare #Economy #Policy #DrugApproval #DigitalPayments #Competitiveness #RegulatoryReform

Eli Lilly's orforglipron just hit a game-changing milestone for obesity and Type 2 diabetes treatment, reports Annika Kim Constantino. This oral pill led to over 10% weight loss and improved blood sugar in a major trial, with easier use than injectables. Could this broaden access for patients wary of injections? Discover more: https://www.cnbc.com/2025/08/26/eli-lilly-weight-loss-pill-orforglipron-clears-trial-paving-way-for-approval.html Great insights by Annika Kim Constantino. #EliLilly #orforglipron #weightloss #diabetes #clinicaltrials #GLP1 #drugapproval #pharmaceuticals #obesity #healthinnovation
Eli Lilly’s weight loss pill orforglipron clears its latest trial, paving way for approval

Eli Lilly now has the clinical trial data required to start filing for approvals of the drug for chronic weight management with global regulators.

CNBC

Gizmodo: FDA’s New Drug Approval AI Is Generating Fake Studies: Report. “CNN spoke with six current and former employees at the FDA, three of whom have used Elsa for work that they described as helpful, like creating meeting notes and summaries. But three of those FDA employees told CNN that Elsa just makes up nonexistent studies, something commonly referred to in AI as ‘hallucinating.’ The […]

https://rbfirehose.com/2025/07/25/fdas-new-drug-approval-ai-is-generating-fake-studies-report-gizmodo/

FDA’s New Drug Approval AI Is Generating Fake Studies: Report (Gizmodo) | ResearchBuzz: Firehose

ResearchBuzz: Firehose | Individual posts from ResearchBuzz

FDA: FDA Embraces Radical Transparency by Publishing Complete Response Letters. “The U.S. Food and Drug Administration (FDA) today published more than 200 decision letters, known as complete response letters (CRLs). The CRLs were issued in response to applications submitted to the FDA for approval of drugs or biological products between 2020 and 2024, marking a significant step in the […]

https://rbfirehose.com/2025/07/18/fda-fda-embraces-radical-transparency-by-publishing-complete-response-letters/

FDA: FDA Embraces Radical Transparency by Publishing Complete Response Letters | ResearchBuzz: Firehose

ResearchBuzz: Firehose | Individual posts from ResearchBuzz
Canada should review how deferiprone was approved, doctors say | The Star https://bit.ly/3ojRBMU #HealthCanada #DrugApproval #deferiprone #UHN #DrugTrials #cdnpoli @canadiangreens @cdnpoli
Drug approval under the microscope as two doctors allege Health Canada received flawed evidence about blood medication

Health Canada’s approval of deferiprone relied in part on data from Toronto hospital patients who received the medication before it was licensed.

thestar.com