EU CLINICAL TRIAL REGULATION CONSULTANCY

We have navigated through the complexities of the EU Clinical Trial Regulation (and CTIS) providing strategic support to our Clients for optimal operational delivery.

SOP WRITING

Operational experts leading operational processes, change management through to implementation ensuring compliance at a systemic level.

CLINICAL TRIAL APPLICATIONS

Expertise in supporting global clinical trial applications, providing a range of support from strategic advice through to submissions and maintenance activities.