Pharmacies are a very important component in the structure of health systems, and their qualified employees have much broader competence than only dispensing medicines recommended by doctors. Pharmacists are able to advise patients on drug regimens and can offer...
In the ever-evolving landscape of pharmaceuticals and clinical research, improving the patient experience remains a critical priority. From the moment patients embark on their clinical trial journey, it is essential to ensure they are well-informed, engaged, and...
The concept of one medicine was invented by Calvin Schwabe in the 20th century. Its underlying assumption is that if humans are able to cure a disease in a particular species, the knowledge obtained from research studies should also be used to help other species....
The protocol is a key document for every clinical trial. It is fundamental to the entire research project, defines the objective and describes the design of the study as well as details of the applied methodology and methods of statistical analysis. It provides...
Translation of regulatory submissions is often perceived as a necessary evil by clinical trial management teams, because it involves considerable financial outlays. Therefore, persons responsible for regulatory submissions are usually under a lot of pressure. Despite...
Different language versions of study-related materials rate among the basic tools used to increase patient diversity in clinical trials. They are of particular importance because language barriers may prevent information about a conducted study from reaching potential...
