Over the last half-century, the landscape of biomedical research has transformed significantly, with commercial entities now dominating the field, often prioritizing profit over knowledge.
In the past, psychiatric research was predominantly driven by academic institutions, with primary investigators managing all aspects of their studies, from hypothesis formation to data interpretation.
The regulatory environment surrounding clinical research has become increasingly stringent, evolving from minimal oversight to a comprehensive framework aimed at ensuring ethical standards.
In my early career, there was minimal oversight in research practices; however, now there are extensive regulations to review ethical and scientific integrity in studies.
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