MFPL’s highly skilled team of medical writers have experience of working on a variety of projects from initial protocol development to clinical study reports and final regulatory documentation listed below:
Our medical writers ensure clear and high quality communications with concerned regulatory agencies throughout the process.
Our Medical writer’s team work directly with our clients to ensure consistency with clients format and style while maintaining full compliance with regulatory requirements and International Conference on Harmonisation (ICH) guidelines, Schedule Y or any other guidelines if required.