ODC BV delivers clinical excellence from first-in-human trials to phase III and Non-interventional clinical studies and medical device trials. We understand that successful clinical trials need expert capabilities but also a partnership you can trust and that provides all the resources you need in one seamless process. At ODC BV we all share great passion for excellence in clinical research.

We believe in clear communication, hard work and are always looking forward. You will realize that our team members don’t hesitate to go the extra mile to provide you with everything you need to reach your goal in time. Whether you need assistance with parts of your trial or require our full services, we’ll provide a fully tailored package to suit your needs.

We cover the way from consultancy to site feasibility and start-up as well as regulatory affairs, medical writing project management, monitoring and site management and pharmacovigilance. By our advisory board we are able to provide you with any kind advice needed. Through our network of partners we can cover all Europe, including all Eastern European countries, North America and Asia Pacific.

We are small enough to care and to be personable, yet large enough to perform well in the largest of studies.

OUR PHILOSOPHY

Our philosophy is to aid the development and implementation of high-quality research studies with our personal consultancy services. We make the process as easy as possible, complying with all regulatory requirements in accordance with ICH-GCP. With strong ties to the academic community, we are uniquely positioned to partner academic institutions, consortia and pharmaceutical companies in the development of clinical and translational trials of novel agents.