We usually run multiple studies around the same time. The studies’ criteria, timelines and dates all differ from one another and can sometimes change. To determine which studies you could potentially take part in we must first analyse the blood sample from your initial screening appointment. If you are eligible for the next stage of screening, we will then send you an informed consent form. This is a document approved by all the relevant regulatory authorities and it will explain in great detail all about the study.
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An average clinical trial length is 11 – 14 days. To apply for FluCamp please complete our online form. We'll call you back within 24 hours to explain the next steps so you can decide if it's for you.APPLY NOW