palleos healthcare GmbH

palleos healthcare GmbH

Discover excellence with palleos healthcare, your trusted full-service CRO in Germany. Our services include phase I – IV, NIS and medical device trials in various indications. Still in preclinical stage or in need of strategic advice? Our experienced consulting team ensures your product development strategy is well aligned with your targets.

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  • Europe

Therapeutic Areas

  • Cardiovascular
  • Dermatology
  • Gastroenterology
  • Infectious Diseases
  • Oncology
  • Respiratory

palleos healthcare is dedicated to offering exceptional services that help you achieve innovations for patients. As a full-service Clinical Research Organization (CRO), we specialize in guiding phase I – IV clinical trials from inception to successful study completion.

We are committed to excellence, offering an extensive range of services that encompass a great range of clinical research. From meticulous project planning to seamless closure, our team excels in Regulatory Affairs, Monitoring, Data Management, Medical Writing & Medical Monitoring, Safety & Pharmacovigilance, Statistics, and Project Management. Tailoring our approach to align seamlessly with your unique project requirements, our experienced team provides professional support throughout your project.

Our clients include big pharma partners, biotech and MedTech companies. Our proven expertise includes large scale interventional trials as well as early-stage explorative projects.  palleos healthcare has cultivated an extensive national and international network, collaborating with diverse service providers throughout the drug and medical device development supply chain. We cover a range of indications with a specialization in oncology.

We invite you to connect with us and explore a partnership for your product development journey.


Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.
Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.
Partners are trained on the functionality of the RTSM Application, process optimization, best practices using RTSM, and scope of RTSM services. This Accreditation teaches Partners to conduct randomization and clinical trial supply management services (RTSM). RTSM Accreditation is dependent on the successful completion of the Rave EDC Accreditation.