Personal commitment and professional expertise for your product
Professional and practical expertise for clinical studies
Our team has outstanding expertise in a wide range of therapeutic areas:
- Pharmaceuticals
- Medical devices
- Digital health applications (DiGa)
- Dentistry
- Allergology (immunotherapy/hyposensitisation)
- ATMP (stem cell therapy, CAR T cell therapy)
- Autoimmune diseases
- Dermatology
- Hereditary metabolic defects
- Immunology (vaccines)
- In-vitro diagnostics (IVD)
- Neurology (CNS)
- Oncology/Hematology
- Ophthalmology
- Orphan/Rare Diseases
- Orthopaedics
- Pediatrics
- Phytopharmaceuticals, homeopathic remedies
- Food supplements
- Rheumatology
- Pain
- Urology
Experience you can rely on – in every study
Reliable partner with practical expertise
Our expertise is particularly useful when we are involved at the start of a clinical trial. This allows us to plan the study design efficiently and purposefully from the beginning, as subsequent adjustments are often time-consuming and costly. At the same time, we also offer our support for specific tasks in the individual phases of the clinical trial. Be it in the area of statistical consulting, medical writing, (pharmaco)vigilance or other specialized tasks: We ensure that every task is carried out with the utmost precision and experience. We are happy to support you in the context of nationally planned studies (DACH), as well as with our qualified and established network in an international context.

About us
CONVIDIA is a member of:
- Cooperation phytopharmaceuticals and
- Supporting member of the Competence Network Lifescience (CONELIS)
-
Innovative Medicine working group at EUCROF
Personal commitment in an interdisciplinary team
We are an independent, competently positioned full-service company for contract research (Clinical Research Organization; CRO) based in Münster, Westphalia, Germany.
We have been supporting clinical trials in a wide range of indications in conventional and innovative therapeutic approaches since 2012. During this time, we have not only found reliable, qualified partners, but have also established clearly structured processes to conduct clinical trials efficiently, successfully and with excellent quality. We always work in accordance with ICH-GCP/ISO14155 and all national and international guidelines.
As a small company, we have a personally committed, professionally excellent and loyal team that identifies with the tasks and requirements of our projects. For us, satisfied employees are the most important prerequisite for satisfied clients: we know our clients and partners and value the trust that comes from long-term cooperation. This is why we value personal continuity in our customer relationships and avoid changing contact persons during or after a project.
Through our high level of identification with the projects and close collaboration, we ensure that every step of the clinical trial is carried out with the utmost precision and care.

Career
Currently we do not have any vacancies
Nevertheless, we appreciate your interest in our company and our services. Perhaps we will get together at a later date!
Contact
We are happy to be there for you personally: Talk to us if you have any questions about us and our services!
We are also always happy to have nice conversations at congresses:
CONVIDIA clinical research GmbH
Urbanstraße 8
48143 Münster, Germany
Phone: +49 (0)251 - 21 401 30
contact@convidia.de