Improving health through science.
We are the World's leading Microbiome Contract Research Organisation (CRO). 80% of our trials yield a positive result for our clients.
Experts in delivering human clinical studies
We design and perform acute, observational, PK, PD, pivotal, efficacy, interventional, safety and tolerability studies to ICH-GCP standards in order to advance research and support evidence-based final product claims.
Clinical Trial Recruitment
Atlantia offers a proven ability to meet recruitment milestones of healthy and pre-disease participants.
Clinical Trial Reporting
The Atlantia Clinical Research team provide a comprehensive study reporting service.
Clinical Trial Conduct
Our unique model maximises control, reduces the risk of data inconsistency, and brings a sense of assurance to our clients dealing with one competent organisation as opposed multiple contract research organisations.
End-to-end services
We are a flexible and dynamic company and we partner with our sponsors, aligning their clinical goals, to deliver the highest quality validation research in accordance to ICH-GCP standards.
Experienced across a broad array of health areas
We are experts at managing every type of human clinical study from design to the desirable outcome, whether this is to obtain a proof of efficacy, substantiate a health claim or simply to gather credible clinical evidence to support your sales and marketing teams.
Want to take part in a food study?
Clinical trials are research studies that explore whether a medical strategy or treatment is effective or if the health claims associated with the product are accurate. The only way that this can be tested for effectiveness and tolerance is with the help of volunteers.
Our Clinical Trial Process
Clinical Design
Study design is a significant phase of any clinical research project. At Atlantia we can plan and guide you to design a successful trial depending on your focus: to increase sales, to obtain a health claim or as a proof of efficacy.
Trial Regulation
Our regulatory services include ethical submissions and approvals as well as regulatory compliance with global health agencies.
Study Recruitment
Atlantia offers a proven ability to meet recruitment milestones of healthy, pre-diseased and diseased participants. We have access to populations of all age groups and we are experienced in recruiting populations from 20 to 600 participants per trial on budget, and on time.
Study Conduct
Our unique model maximises control, reduces the risk of data inconsistency, and brings a sense of assurance to our clients dealing with one competent organisation as opposed multiple contract research organisations.
Trial analysis
At Atlantia your clinical data is at the centre of our service. When the samples are collected either during study visits or remotely they are prepared and stored at our facilities at -80*c, -20*C or refrigerated temperature and analysed by our research partners.
Study reporting
The Atlantia Clinical Research team provides a comprehensive study reporting service. Our statisticians adhere to ICH-GCP standards to produce a statistical study report, and if the client requests, a full clinical study report.
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The results speak for themselves
Our team has put together these clinical trial case studies in multiple
topics to help you understand how we have assisted other sponsors
in the past to tailor their clinical research programs.
Get in touch!
Our team can guide you. Schedule a meeting with our research experts to discuss your clinical research program today.
