Why Choose Us?
Why Choose Us?
Akela offers personal attention, continuity and accountability. Short set-up times and rapid response are key elements in our service.
Testimonials
Testimonials
"I have no hesitation in recommending Akela for performing Clinical Research oversight...."
Contact Us
Contact Us
Telephone or email for information on our services or career opertunities.
Site Initiation

We will collect and verify your essential documents.

We will coordinate your third party vendors/suppliers.

We will organise the trial master file and compilation of investigator site files, and site/study reference manual.

We will manage the investigator contracting process, ethics committee submissions and R&D approvals.

Finally, we will ensure the site is ready to recruit, including Study Site Coordinator training (if required).


Telephone enquiries:   +44 (0) 1837 82165

    Protocol Review

    Site Selection & Qualification

    Site Initiation

    Site Management

    Vendor Selection

    SOP Writing

    Project Management

    Monitoring

    Clinical Operations Advice

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