https://lane-medical-writing.com/frequency-clinical-trials-data-making-public-domain/?utm_source=rss&utm_medium=rss&utm_campaign=frequency-clinical-trials-data-making-public-domain Freelance bilingual medical writer based in Lyon Tue, 01 Aug 2017 15:40:11 +0000 hourly 1 https://wordpress.org/?v=3.8.41 https://lane-medical-writing.com/frequency-clinical-trials-data-making-public-domain/#comment-38 Tue, 01 Aug 2017 15:40:11 +0000 http://lane-medical-writing.com/?p=957#comment-38 Indeed, this is the theory. This recent article in BMJ describing an audit conducted by Ben Goldacre et al provides interesting and up-to-date reading: Pharmaceutical companies’ policies on access to trial data, results, and methods: audit study. BMJ 2017;358:j3334

]]> https://lane-medical-writing.com/frequency-clinical-trials-data-making-public-domain/#comment-37 Tue, 01 Aug 2017 11:14:50 +0000 http://lane-medical-writing.com/?p=957#comment-37 Data providers create the protocol section and register summary protocol information when their studies are initiated. Subsequently, data providers create the results section for these study records when data collection for at least one primary outcome measure is complete.

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