There is no question that publishing health research is important. Not only are you able to communicate your findings to the world, but also your articles will become immediately citable. Most importantly, a great number of issues have become prominent, such as newly-emerging epidemics and it is needless to say that solutions are welcomed. Running clinical trials is not exactly easy, but neither is preparing the raw data for publication. If you want to publish your research in a journal of health research or to be listed on http://www.scientia.global/
, you need to keep in mind the following guidelines:
Anonymise the clinical reports
It is important not to forget that when you are carrying out clinical reports you must preserve the patients’ anonymity. What this implies is remove personal data prior to publication. Whatever you do, you should not rush onto publishing your findings. Releasing certain data will not only expose your patients, but also it will harm your research. The results of the clinical trial can be copied with great ease and this will affect the understanding of your discovery.
Some publications of health research may require you to transfer the copyright for the supporting data. You remain the owner of the datasets, but one of the copyrights is granted to the publisher. Basically, you are giving the journal the right to publish your work. On the other hand, if you do not want the datasets to be published, all you have to do is separate it from the scientific article.
Have an editing firm read your manuscript
One of the most important features of scientific writing is clarity. However, in the medical field there is a tendency to use language that is not really suitable for non-professionals. While you are writing for your peers, you also want to get your message across to regular people as well. A good idea is to hire a specialised firm to proofread and maybe edit your manuscript. Your document will be thoroughly analysed and you want the text to be free of errors.
Make sure you comply with clinical trial regulation
The last thing you need to do is make sure that the clinical trial is in compliance with EU regulations. When it comes to publication of clinical data, especially when it comes to human medicines, there is a criterion that needs to be met. You will find all the information you need online.