Why Use GFA?

What sets us apart from other consultancies and CRO's?

Our team is sufficiently big (22 staff) to give confidence of resource, but still small enough to care.
GFA concept is to maintain close links between our regulatory and clinical research teams, such that all staff develops a good understanding of the needs of the whole project team.
In these days of increased regulation - and of the closer links between the team running a clinical trial and the team seeking regulatory approval, this is ever more important to ensure trials run smoothly.
Our clinical research team is focused on early stage Phase I and II trials - and to achieve this we employ only experienced staff who can think on their feet to trouble shoot during these early studies.
Our regulatory team's breadth of experience ensures successful submissions of Orphan Drug applications, Clinical Trial authorisation applications and Marketing Authorisation Applications in the EU and USA.

GFA Offers: