I have to find a topic for my master study (Biotechnological Qualitymanagement). The planned direction would be Good Clinical Practice / Clinical Trials.
A potential topic would be about the role of sponsorship in non-commercial and commercial clinical trials regarding Good Clinical Practices guidelines.
Any comparative analysis of Adverse Events registered within clinical trials and in routine practice. Such studies are extremely important but still practically absent.
the question is not the latest, but I hope my answer can be intersting for you:
Most studies state that they are performed with regard to GCP. In reallity, there is a huge gap between the needs for GCP and the quality of performed studies. i Think this would be a great master thesis.