The master protocol pools resources and infrastructure for multiple clinical investigations. This modular approach accelerates development and meets the requirements of the MDR regulation.
Master protocol: a pillar for structuring clinical investigations. Read more "
The PSUR becomes mandatory for Class IIa and higher medical devices under MDR. Find out how to structure this safety report and turn it into a strategic asset.
MDR Regulation: everything you need to know to write a compliant PSUR. Read more »
Biostatistics transforms raw data into robust clinical evidence. Discover its role in study design, data analysis, and benefit/risk assessment of medical devices.
The importance of biostatistics in clinical research Read more »
Continuing education reduces the environmental footprint of clinical investigations while improving talent retention (94%) and team efficiency.
Continuing education: a lever for eco-responsibility in healthcare Read more »
Digitization reduces the healthcare sector's carbon footprint: 15 times less CO2 for a digital page vs. paper. Telemedicine and EDC limit travel and resources.
Digitization to reduce carbon emissions: myth or reality? Read more »
