Adaptive clinical trials are defined as studies in which accumulating data is used to decide how to modify aspects of the study as it continues, …
The first reference to the creation and usefulness of a patient electronic medical record may have been the visionary writing of Robert Ledley and Lee …
The Human Research Ethics Committee (HREC) at University of the Witwatersrand (WITS), has regulated that all biobancks being accessed by researches submitting protocols for review …
Immunoglobulin E (IgE)-mediated allergic conditions are increasing worldwide. They affect the quality of life of millions of individuals, causing enormous costs for society. In her …
With its population of 145 million and total pharmaceutical sales of almost 29 billion dollars in 2013, Russia today is among the world’s ten largest …
Often asked ‘How do you recruit patients?’, Helen West of MMG explains in her article that the emerging focus on patient-centricity may help foster a …
An important part of clinical study reporting, safety narratives should be prepared for all phases of clinical studies, whether conducted in healthy volunteers or in …
All sponsors try to optimise their resources when conducting clinical trials, and sometimes the desire to reduce study budgets leads to the selection of less …
China’s pharmaceutical market has expanded dramatically in the past twenty years and is expected to become the largest in the world by the year 2050. …
Hypertension, the leading cause of cardiovascular disease and deaths globally, is a well-established, easily detected, and modifiable risk factor for cardiovascular disease. Dr Winter and …
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