AK Clinical Research provides clinical site services, specialising in conduct of virtual and decentralised clinical studies. We operate as a private site, outside the public health system, allowing us to expedite the regulatory and set up processes, getting you to first participant enrolled sooner.

We are experienced in delivering phase II-IV interventional studies, capturing real world evidence and conducting observational research in the usual clinical setting.

AK Clinical Research has partnered with an extensive network of highly trained and experienced investigators and study coordinators to conduct clinical trials across a broad range of therapeutic areas as well as extending into general practice to facilitate faster trial recruitment.

• Centralised feasibility. AK Clinical Research coordinates all aspects of study feasibility, site selection, collection of ethics and regulatory documents, SIV and investigator training across all our network.
• Expedited Ethics. With many years’ experience in ethics applications for multisite applications, we manage the ethics approval process efficiently.
• Quality Assured. Our program director is highly experienced in clinical trial delivery, having worked with Sponsors and CROs for over 25 years. With experience in site FDA inspections and audit readiness, your trial will be managed to strict GCP and regulatory compliance.

Contact us now to discuss how we can assist with your clinical study site needs.