Working with Authors

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There's been a lot of back and forth in the media about the pharmaceutical industry, including GSK, and the role of "ghostwriters" in preparing articles for peer-reviewed scientific journals. You should know where GSK stands.

 

While the requirements of medical journals have evolved over the years, our current policy is that a medical writer's substantive assistance in the content of an article is documented either by authorship or in the acknowledgements section of the publication.

 

We work closely with investigator authors. GSK upholds strict guidelines to ensure that the development of study manuscripts is led by investigators who have made a substantial contribution to the study. That includes drafting the manuscript or revising it critically for important intellectual content, retaining final approval authority.

 

We continually review our practices. We have our own guidelines on this topic.  They reflect those established by the International Committee of Medical Journal Editors and PhRMA Principles on Conduct of Clinical Trials and Communication of Results. We continually review our guidelines to make sure they cover current issues.

 

We want to be transparent about whose work is represented and that the investigator is in control of the contents.

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About this Entry

This page contains a single entry by Mary Anne, GSK Communications published on August 20, 2009 4:29 PM.

Leading by Example was the previous entry in this blog.

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