From now on, the website has a new design and an even clearer structure.

Real world data (RWD), which is data from actual patient treatments, provides valuable information on safety and effectiveness of innovative ...

Sponsors can sometimes require a qualitative research study protocol to be drafted using a clinical trial protocol template, within which many of the sections are not applicable. It is here that ...

The evolution of protocol management within eQMS represents another significant advance in clinical trials. Version control ...

How did we get here? February marks five years since Brexit became official. Here are some key developments since the EU-UK ...

Large language models (LLMs) are poised to have a disruptive impact on health care. Numerous studies have demonstrated ...

These tips have been adapted from Jacob and Furgerson’s (2012) guide to writing interview protocols and conducting interviews for those new to qualitative research ... of the relevant information ...

Ethics and dissemination The protocol steers the collection of primary and secondary data across the study sites. Research ethics board approval ... Executive summaries are based on a global template ...

Even though the European Alliance of Associations for Rheumatology has identified mediators of OA outcomes as an important research priority to enable individualised healthcare in the future,4 52 57 ...

19. Keep the BSB informed of any changes in your supervisor to avoid delays in your practising certificate processing. 20.

Observational studies are critical tools in clinical research and public health response, but challenges arise in ensuring ...

A far shorter, simpler, and less toxic treatment protocol for patients with triple-negative breast cancer produced outcomes ...