The goals of the Drug Center (CdF) are to provide methodological and regulatory expertise for the conduct of clinical research, both by the San Raffaele Group and by outside companies.
These services range from the design and coordination of research projects to project management of studies;from analyisideidatie finalstudy reports to the development of regulatory dossiers (registration, pricing and reimbursement).
The CoF works in perfect harmony with the Clinical Trial Center, which operationally supports all phases of the design, management and conduct of clinical trials, with a view to providing a high-quality clinical research service.
The Clinical Trial Center (CTC) was established within the San Raffaele Group to support clinical research activities conducted in the areas of expertise.
The various departments have organized themselves independently, aware of the importance of having dedicated resources for this activity. The CTC harmonizes intra-departmental activities and thus aims to support clinical units in the preparation, conduct and completion of clinical studies, whether interventional or observational. The CTC has internal regulations regarding the functions and responsibilities of all members belonging to the Team and has developed all the necessary SOPs for carrying out its activities, prior to the initiation of studies, during their execution and at the conclusion of clinical research activities.
