There are several reasons to enlist or register clinical trials on a public registry. Here we note some key considerations.
Several countries, like the United States and European nations, the regulatory body authorities need clinical trial information, even the results, must be disclosed.
The International Committee of Medical Journal Editors (ICMJE) in their policy mentioned that that all medical journals must need the registration of clinical trials on WHO’s Primary Registry as a precondition to publications.
Some companies, academic institutions, and other research facilities have policies to disclose clinical trial information. The policies state that all legal necessities must be met, and some policies are more than the legal obligations.
Many industrial organizations have their policies on the carrying out of clinical trials and data sharing like the Pharmaceutical Research and Manufacturers of America (PhRMA) PhRMA Principles on Conduct of Clinical Trials, the European Federation of Pharmaceutical Industries and Associations EFPIA policy statement on Clinical Trials Regulation and Biotechnology Industry Organization (BIO) BIO Principles on Clinical Trial Data Sharing, only to mention just a few. It is safe consideration that if you belong to any industry organization, there is a policy on clinical trial disclosure reporting of results.
In 2014, the National Institutes of Health (NIH) suggested a policy saying all studies which are fully or partially funded by the NIH, must be registered and basic results are disclosed.
Ethics and more:
Several organizations stated the need for ethical conduct during human research. The Declaration of Helsinki, which was first adopted by the World Medical Association (WMA) in 1964, was amended in 2013 with specific understanding and transparency.
The AllTrials initiative asks for all previous and present clinical trials to be registered with reports of their full methods and summary results.
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