Browsing Dr. Peter Doshi by Title
Now showing items 10-29 of 84
|Calibrated response to emerging infections |
|Canada finally opens up data on new drugs and devices: Other regulators should take note of Health Canada’s substantive reforms |
|CDC tightens controls on scientists’ communication with news media |
|Challenges of independent assessment of potential harms of HPV vaccines |
|Cherry-picking by trialists and meta-analysts can drive conclusions about intervention efficacy |
|Clinical study reports of randomised controlled trials: an exploratory review of previously confidential industry reports |
|Clinical trial data: get them while you can |
|Contradictory findings on efficacy of neuraminidase inhibitors not cited |
|Contribution of industry funded post-marketing studies to drug safety: survey of notifications submitted to regulatory agencies |
|Convicting Zika |
|Correction: Integrating multiple data sources (MUDS) for meta-analysis to improve patient-centered outcomes research: A protocol [Syst Rev. 4, (2015) (143)] DOI: 10.1186/s13643-015-0134-z. |
|Covid-19 vaccine trial protocols released |
|Covid-19: Do many people have pre-existing immunity? |
|Covid-19: Should doctors recommend treatments and vaccines when full data are not publicly available? |
|Data too important to share: do those who control the data control the message? |
|Defining antibiotic effectiveness and resistance: how a private party may soon rule judgments over susceptibility testing |
|Determining the infectious potential of individuals with positive RT-PCR SARS-CoV-2 tests |
|Does oseltamivir really reduce complications of influenza? |
|EFPIA-PhRMA's principles for clinical trial data sharing have been misunderstood |
|The elusive definition of pandemic influenza |
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