Guest guest Posted January 8, 2011 Report Share Posted January 8, 2011 Respected members, US FDA recommended principles of "Good Reprint Practices": Organizational publications which are peer-reviewed and not funded by the manufacturers of the product in the manuscript. The manufacturer should not influence directly, or any individual involved in the writing, editing or publishing of the scientific information. The information in the scientific or medical journal article or reference publications should not be false or misleading and should be derived from adequate and well-controlled clinical investigations. The information should not pose a significant risk to the public health. Publications which do not qualify for dissemination to healthcare professionals include letters to editors, abstracts of publications, results of Phase I trials and publications without relevant investigations or data. Scientific information should not be presented in a form that might bias the judgment of the physician and should be accompanied by the approved labeling of the drug or the device. Regards Dr Sanjay Yallappa Choudhari JR2,Dept of Pharmacology GMC, Nagpur Quote Link to comment Share on other sites More sharing options...
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