We are focused on your clinical trial
Our goal is to support the people and processes that play an integral role in ensuring the success of your clinical trial. The investigator site is the front line of your trial. Our team will help your site staff manage the important processes of patient enrollment and treatment so that they feel in complete control. This will result in better site performance and improved overall compliance.
We understand the study-specific challenges sponsors currently face with patient enrollment and randomization, assignment of medication and overall control of the clinical supply chain. Whether you are developing a vaccine or biotech product, or running an early- or late-phase study, our extensive clinical operations and clinical supply experience will give you the tools you need to address the specific dynamics and challenges that all types of trials will present.
Experience, knowledge and solutions
Cenduit’s heritage has provided us with an unmatched pool of expertise in clinical trial management. We have in-depth insight into both clinical operations and clinical supply chain management. When you present us with your clinical protocol, we will use this knowledge and experience to determine the most effective way to control the processes of patient enrollment and drug assignment in your specific trial.
Cenduit has significant regulatory expertise and can guide sponsors on the latest GxP requirements for IRT-driven clinical trials. Our team will design a smart, user-friendly system tailored to the needs of your specific trial with the investigator sites in mind.
Our project management staff is an extension of your clinical team. They are available to provide advice and support throughout your trial and are responsible for ensuring patient randomization and treatment processes run smoothly. Cenduit’s global support network is located in all the key markets, including the United States, Europe and Asia.
Ensuring that a patient is randomized into the right treatment group and receives the correct medication in a clinical trial is critical, not only for the trial itself but more importantly for the patient.
For this reason, quality assurance plays a vital role in the delivery of our service and the successful management of your trial. We will always assign patients to the right treatment group, we will always assign them the correct medication, and we will always ensure absolute compliance with the requirements of the protocol.
Information and technology
We continue to invest in the latest technology and systems that enable sponsors and sites to seamlessly randomize patients and manage drug supply. The global availability of the Internet and the ever increasing use of mobile applications are transforming the solutions that we are able to provide sponsors and site users.
Cenduit’s reporting module allows for easy access to data and the ability to analyze, filter and present the information on your desktop or mobile device anytime and anywhere. As a result, sponsors and sites stay in control and will have better visibility on the progress of the trial:
- Intelligent reports that provide useful information for decision making
- Data available across the study at country or site level
- Reports that are fully configurable by the user