Clinical Research Insights
Clinical research is an essential aspect of medical advancement, focusing on the study of diseases and development of new medical treatments. It involves human participants
In the world of clinical research, Good Clinical Practice (GCP) is a fundamental framework that ensures the integrity and ethical conduct of trials. For more
Welcome to our blog, where today we will delve into the fascinating world of data management in clinical research. In this fast-paced era of technological
A medical writer is responsible for producing well-structured documents presenting scientific, clinical, educational, or promotional information clearly and concisely. In clinical trials, delivery of these
Medical writers communicate clinical data and various findings in medicine to a wide range of audiences and within the scope of a number of different
Medical writing offers an opportunity to learn about various health fields, medical conditions, as well as drugs, medical devices and treatments. There is a wide
An essential, and often overlooked part of the work on clinical trials is medical writing. It is involved at the start and end of the
The new MDR requires small to midsize medical device companies to take over sponsor responsibilities for their clinical trials. Some companies find they cannot take
ICH GCP and ISO14155 defines the term monitoring as “The act of overseeing the progress of a clinical trial, and of ensuring that it is
“Is it equivalent?” As a medical device manufacturer, you are very aware of MEDDEV 2.7/1 rev. 4. from 2016. Following this document when planning and
