Dr. Catherine Kennedy

Clinical trials are conducted as part of the clinical development of investigational drugs to assess their efficacy and safety profiles. As trials progress, it is essential that the drug safety profile is thoroughly mapped to provide a detailed record of the risks to the subjects participating in the trial. This information is required in the form of the annual submission of a regulatory document  detailing to regulators and other external parties the results of safety information...

Healthcare content marketing  is a strategy used to entice your target audience into engaging with your content and, therefore, the...

The peer review process forms a fundamental aspect of scientific research, acting as a quality control measure to ensure that research is...