Biotrial is a full-service CRO that provides end-to-end clinical trial management services for patients. We have a strong network of Key Opinion Leaders, worldwide partnerships, and a full range of services to offer the best solution for conducting clinical trials in patients.
No matter the therapeutic area you work on, you can rely on our global experience to get the right solution for your project. We have a proven track record of success in a wide range of therapeutic areas, including:
Our healthcare solutions span medicinal products, medical devices & diagnostics, and digital products & apps. We have expertise in a variety of compounds, including small molecules, biologics, and gene therapy products. We also have expertise in the development and use of medical devices and diagnostics. We are committed to staying ahead of the curve and incorporating the latest innovations and trends into our services.
We have a global network of sites and partners and can accompany you, both locally and worldwide, regardless of the geographical location of your clinical trial.
In the past 5 years, we have covered over 50 patient trials in over 20 different countries with the experience and expertise to help you conduct your trial smoothly and efficiently.
Our experienced project management and monitoring team applies a patient-centric approach to ease the patient’s day-to-day life and to ensure patient retention leading to the smooth conduct of your trial. We understand that patients are the most important stakeholders in any clinical trial, and we work hard to make the process as easy and convenient for them as possible.
We provide a variety of solutions that can help to improve the patient experience, including:
Biotrial has built a strong network of experts in many therapeutic fields and in many countries. We can connect you with the right experts to help you with your clinical trial, regardless of its stage or therapeutic area.
We can help you assess the feasibility of your clinical trial and provide advice on the best way to conduct it. We have a deep understanding of the regulatory landscape and can help you to navigate the process smoothly.
Our experienced phase I CPU nurses can lead the clinical sites and help them collect robust clinical data. We have a team of nurses who are experts in the conduct of phase I clinical trials, and we can provide them to your sites to ensure that your trial is conducted safely and efficiently.
We can provide end-to-end support for your clinical trial, from submission to execution. We have a team of experts who can handle all aspects of your trial, including regulatory affairs, pharmacovigilance, medical monitoring, and pharmaceutical management.
