Clinical Development Planning

SFS can be a partner of choice from the beginning of the study, putting our knowledge and experience at sponsor side to help him to be aligned with legal requisites but also to accomplish the objectives as soon as possible.

We develop
protocols, investigator brochures, informed consent forms, drug labels.

We check
the initial documents and provide feedback and consultancy to start the clinical trial.

We provide
experience, knowledge and know-how in every steps of the clinical trial.