Clinical trials play a crucial role in the development and approval of new medical treatments and drugs. As technology continues to advance, Clinical Trial Technology …
When patients receive a prescription drug or biological product in an outpatient setting, it may be accompanied by one or more types of written information …
A Solution for Sparse Evidence, Heterogeneous Studies, and Disconnected Networks If there is a variety of treatment options in a specific disease area, decision-makers require …
ISO/IEC17025:20171 is the international standard that specifies the general requirements for the competence, impartiality and consistent operation of laboratories. It can be used by laboratory …
Improving Access and Participation in Clinical Trials in Ireland, a Patient-centred Digital Health Platform Across Europe, we continue to see a declining trend in the …
Using agile methods, and starting with CMC post-approval submissions, an innovative team has brought the benefits of cloud-based RIM to users throughout the world. In …
Expert committees are a critical component in the success of a clinical trial. By turning to third-party providers to manage these services, sponsors can enhance …
In an era of rapidly evolving information and ever-burgeoning scientific innovations, it can be disheartening to witness the persistent lack of trust in the scientific …
With the recent advent of adeno-associated, virus-based gene therapy treatments, limb-girdle muscular dystrophy (LGMD) is currently attracting the attention of the biopharmaceutical industry, especially with …
According to recent forecasts by Fortune Business Insights, the global clinical trials market is projected to reach nearly $100 billion in 2030. That represents huge …
Journal For Clinical Studies has a distinguished editorial advisory board providing the best guidelines for global clinical trials. Your resource for Multisite Studies and emerging markets.