Conducting clinical trials is an essential aspect of carrying out business for pharmaceutical and healthcare companies. It is well-known that the entire process is also extremely expensive. It includes designing the scope of the trial, creating the inclusion/exclusion criteria for patient recruitment, managing data collection, performing analysis on data, and many other processes.

Each process has to be carefully executed and recorded to ensure that FDA submission is successful and the drug or treatment in question is approved for mass distribution. The entire process looks quite straightforward. The drug development journey should ideally follow this path:


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