Browsing Dr. Peter Doshi by Title
Now showing items 45-64 of 84
|Integrated Drug Reviews at the US Food and Drug Administration-Legal Concerns and Knowledge Lost. |
|Integrated Drug Reviews at the US Food and Drug Administration-Reply |
|Integrating multiple data sources (MUDS) for meta-analysis to improve patient-centered outcomes research: a protocol for a systematic review |
|Is this trial misreported? Truth seeking in the burgeoning age of trial transparency |
|Medical response to Trump requires truth seeking and respect for patients |
|Multisystem failure: the story of anti-influenza drugs |
|Neuraminidase inhibitors for influenza: a systematic review and meta-analysis of regulatory and mortality data |
|Neuraminidase inhibitors--the story behind the Cochrane review |
|No correction, no retraction, no apology, no comment: paroxetine trial reanalysis raises questions about institutional responsibility |
|Noninferiority Trials [letter to the editor] |
|North American regulatory agencies can and should make clinical trial data publicly available |
|Open data 5 years on: a case series of 12 freedom of information requests for regulatory data to the European Medicines Agency |
|Oseltamivir for influenza in adults and children: systematic review of clinical study reports and summary of regulatory comments |
|Pandemrix vaccine: why was the public not told of early warning signs? |
|Patient consent to publication and data sharing in industry and NIH-funded clinical trials |
|Popular and scientific attitudes regarding pandemic influenza |
|The possible harms of statins: What do product labels, patient package inserts, and pharmacy leaflets tell us? |
|Preventing flu-like illness: Reason for optimism |
|The problem with US website for collecting adverse events after vaccination is resolved |
|Putting GlaxoSmithKline to the test over paroxetine |
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