Medfiles offers comprehensive services for phase I–IV studies for human and animal medicinal products, medical device investigations, and food and nutrition studies. We provide you flexible solutions for a complete package extending from study planning to final reporting, including protocol preparation, project management, monitoring, data management, and statistical evaluation.
Our services also include consultation sevices, preclinical study plans, formulation development, manufacturing of investigational medicinal products (IMPs), QP certification, development and validation of analytical methods and stability studies for IMPs. Our personnel undergoes continuous training and we follow update of regulations carefully to ensure that you receive services of the highest quality.
Medfiles offers clinical research and development services such as:
- Early-phase guidance
- Study planning & feasibility
- Protocol, medical & report writing
- Clinical study applications
- Phase I–IV clinical studies
- Project coordination
- Data management & statistics