Patient Trial Management

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.


added values

  • End-to-End services: We will offer a complete set of quality services available individually or as part of a full-service package. 
  • Expertise in many therapeutic areas: We have expertise in a wide range of therapeutic areas.
  • Expertise in many different types of compounds: We have expertise in a variety of compounds, including small molecules, biologics, and gene therapy products.
  • International reach: We have a global network of sites, allowing us to conduct clinical trials in patients around the world.
  • Patient-centric approach: We are committed to a patient-centric approach to clinical trial management. We work closely with patients to ensure that their needs are met and that they are comfortable participating in the trial.

End-to-End services

  • A complete set of services available individually or as part of a full-service package.
  • We can manage a study globally end-to-end: Study design & protocol development, feasibility & site qualification, regulatory submissions, site management, clinical monitoring, medical monitoring, pharmacovigilance, bioanalysis, pharmacokinetics, data management, biostatistics, medical writing, core lab.

Therapeutic Areas

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:

  • Gastroenterology
  • Hepatology
  • Nephrology
  • CNS
  • Oncology
  • Hematology
  • Cardiovascular
  • Infectious disease
  • Dermatology
  • Respiratory
  • Rare disease
patient trial management biotrial

In various types of compounds

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.


Anywhere in the world

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:

  • ePRO/eCOA: Electronic patient-reported outcomes (ePRO) and electronic clinical outcome assessment (eCOA) systems allow patients to self-report their symptoms and progress through the trial, making it easier for them to participate.
  • RBM: Risk-based monitoring (RBM) is a system that uses data analytics to identify patients who are at risk of dropping out of the trial.
  • eConsent forms: Electronic consent forms allow patients to consent to participate in the trial online, making it more convenient for them.
  • CTMS: Clinical trials management systems (CTMS) help us to manage the data from your trial, making it easier for us to track patient progress and ensure the smooth conduct of the trial.

Added values


Access to KOL’s

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.


Feasibility & advice

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.


Support of our phase I CPU nurses

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.


End-to-end support

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.

Participate in a clinical trial

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