Integrity of Randomized Clinical Trials (Original PDF from Publisher)

Integrity of Randomized Clinical Trials

Scientists are expected to be more open and accountable now than they have ever been. The public anticipates significant benefits from the creative contributions produced by researchers, and the pursuit of knowledge creation holds a unique position on a global scale. Therefore, it is more crucial than ever that research integrity be expressly guided by ethics, transparency, and professionalism.

Clinical trial integrity is typically not covered in medical training, whether at the undergraduate nor postgraduate levels, despite the obvious significance of developing a basic grasp of clinical trials in the context of health research and innovation. By presenting best practice standards to enhance the caliber, transparency, and reliability of clinical trials, this new book fills a need in the market and offers a curriculum to close this gap.

The first book about the integrity of clinical trials
gives precise instructions on how to maintain integrity in peer review, trial evaluation, and the examination of complaints pertaining to clinical trial misconduct.
teaches and assists researchers worldwide in conducting trials in an ethical manner.
guarantees that the growing need for open documentation of every facet of a clinical trial’s lifetime can be satisfied.

In addition to being a vital resource for medical journal editors and peer reviewers, clinicians who recruit patients for clinical trials, pharmaceutical industry professionals, patient and public representatives who participate in clinical trials, systematic reviewers, authors of guidelines, funders, and regulators of clinical trials, this book is required reading for master’s and doctoral students enrolled in courses in clinical trials, epidemiology, and medical statistics.