In this blog, we provide a brief overview of the multiple peaks in pharmacokinetics studies, how to handle and the potential impact on study outcomes. In the pharmacokinetics (pharmacokinetic) study, a multiple peaking phenomenon refers to the occurrence of more than...
In clinical research, careful and organized documentation is crucial to maintaining trial integrity and participant safety. Essential documents encompass a range of documents that individually and collectively enable the evaluation of the conduct of a clinical trial...
Diseases have been with mankind since the beginning of time, and medicines have helped countless people to overcome them. Being cured of diseases with the help of drugs is almost everyone's wish. The development of modern science and technology has brought with it a...
The Role of Clinical Scientists at BioPharma: Looking for answers to unresolved questions about human health, contributions to medical advancements, and spearheading innovative research? These are just “a few of the daily work tasks” of clinical scientists. In this...
In this blog, we provide a brief overview of the notion of statistical power, along with factors that can impact it. The notion of statistical power is one of the critical points that should be taken into account when carrying out studies that require statistical...
Vomiting is one of the most common adverse events (AE) in clinical trials. While most AEs are mild and self-resolving, cases of moderate to severe emesis are not infrequent and can impact the safety of participants and the integrity of study data. Using antiemetics is...
