Our expert research team will work with sponsor(s) to design and conduct a study most suitable for their investigational product, agreeing and applying the most suitable diagnostics. We can statistically power your study to ensure that your objectives are achieved and reported in accordance with regulatory guidelines.
Such as gut mobility, video camera endoscopy (VCE), constipation, IBS/IBD, GERD, barrier function.
Such as respiratory (URTI), urology (UTI), dysbiosis, cold and flu.
Cognitive decline, self-reported memory loss, sarcopenia, muscle function, bone and joint function.
Cognition, stress and mood, sleep, gut-brain axis.
Flow mediated dilation, blood pressure, triglycerides.
Weight management, pre-Diabetes & Diabetes, blood Lipids.
Skin microbiome, transepidermal water Loss (TEWL), hydration, wrinkles.
Probiotics/ Prebiotics, Skin Microbiome, Gut Microbiome, Women’s Health, Biotherapeutics.
Our team is experienced in working in even more health areas and endpoints, reach out to learn more.
At Atlantia we assess changes in biological parameters with both objective and subjective assessments:
• Subjective assessments such as well-being, quality of life and eating habits using validated questionnaires
• Objective parameters which assess specific biomarkers for each indication through a variety of samples and methods. We can collect and process hair, blood, feacal, urine, skin, saliva samples or vaginal swaps as required by the study
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.
Our regulatory services include ethical submissions and approvals as well as regulatory compliance with global health agencies.
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.
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.
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.
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.
Our team can guide you. Schedule a meeting with our research experts to discuss your clinical research program today.
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.
