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.
Atlantia maintains no rights to Intellectual Property generated from the study. We maintain ownership over procedures and software, but not the data generated.
The purpose of a clinical study report is to compile the whole clinical trial process.
We can help you to publish your study in peer-reviewed journals.
Our team can guide and assist sponsors in creating materials to increase the outreach of the research project.
If required, our scientific team can prepare a CSR. A draft would be circulated to the sponsor for initial review. A final draft would be prepared with comments, corrections and amendments included. The results would be presented in a final study close out meeting.
We can help our clients with the publications of results and the registration of trials. We can approach and format clinical outcomes in accordance with publisher's requirements and manage the process entirely. Our published work can be consulted under our Publications page.
Our team can assist you in developing a strategy to enhance the outreach of the study results depending on your target audience. Our design team is able to develop in-house graphics as well, some examples are:
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.
