Our key areas of expertise include:
We can also manage projects from other medical fields.
Our experienced, GCP-accredited clinical trials team of medical doctors and engineers has a deep understanding of medical devices and clinical trial processes.
We cooperate with various manufacturers but retain the right to choose the optimum solution for each clinical trial. This makes us a unique, highly specialised partner for CROs and sponsors, not only as an equipment provider, but also as an experienced (and again independent) medical device consultant.
All our procedures are GCP compliant and validated in real clinical environments (by our own Clinical Trials Evaluation Centre).
Our R&D department allows us to efficiently customise existing serial production devices for aspecific trial needs.
Continual collaboration with medical scientists and experienced clinical sites enables us to provide a dedicated, effective and optimised solution for each project.
We use state-of-the-art, customisable and scalable IT infrastructure based on the world’s most trusted and secure cloud platform. All project data are immediately at our partners’ fingertips in the desired format.
A dedicated project manager coordinates each project from beginning to end. We’re located in the heart of Europe with subsidiaries in Germany and Poland.
Innovation is our passion – not to mention our company’s mission. We strive to provide the most innovative solutions for the clinical trials industry, continually introducing new, modern tools to provide outstanding service. Besides traditional face-to-face meetings and training, we specialise in dedicated tele-medical training, instructional videos, interactive SOPs and remote maintenance.
Since 2001, PRO VITA has specialised in pulmonary function testing solutions, providing a complete range of diagnostic devices, from basic devices up to the most advanced, complex PFT systems.
PRO VITA works closely with the leading pulmonary diagnostic manufacturers but remains independent, offering the right solution for every clinical trial and project.
Our independency, unique experience and in-depth medical knowledge results in incomparable, high-quality services for pulmonary clinical trials.
Our team has immediate access to real clinical environments thanks to our close collaboration with leading pulmonary professionals and medical universities. This allows the efficient, proactive creation and verification of each diagnostic solution.
*With our CTS1 Team, you can be sure our experts are always available.
Years of clinical trial experience
Projects completed
Support & service availability
We can
meet any challenge related to pulmonary function testing.
A challenge in every trial protocol is finding the optimal diagnostic methods for a specific group of patients.
Key to a study’s success is optimising patient workload and compliance during the trial.
We operate our own pulmonary clinical trial centre with more than 20 years of experience and dozens of completed projects, specialising in asthma, COPD and other respiratory diseases.
Together with our expert team of engineers, we offer an industry-leading, comprehensive analysis of the trial protocol. We perform our analysis on a pilot group of patients who comply with the protocol and we examine every aspect of their workload associated with the trial.
We then produce a comprehensive pre-study feasibility report summarising all the diagnostic and reporting procedures. The report covers patient workload and satisfaction, clinical site workload and a summary of the challenges, difficulties and potential threats to the study’s overall feasibility.
*If you need another PFT modality, please do not hesitate to contact us.
We know
service quality and responsiveness are crucial during clinical trials.
We recommend three simple steps for starting a dialogue between us:
