It depends on the type of study and the estimated timelines. If you send us the protocol synopsis, we can give you an estimated budget so that you can get a general idea. The more information you provide us, the more detailed your budget will be.

Yes, our Quality Management system is certified by the ISO 9001 2015 standard.

In addition, all our staff are trained in Good Clinical Practices and in the ISO 14155 2020 standard Clinical investigation of medical devices for human use; and we comply with the General Data Protection Regulation (2016 679 EU GDPR).

We have worked in almost all therapeutic areas and we have extensive experience, mainly in oncology, ophthalmology, cardiology, endocrinology, traumatology, rare diseases, neurology, pneumology and hematology.