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About us

Our medical trial and observational study preparation and execution team is recruited from MUC Research and Clinovate and has been working together since 1999.

Your VALHALLA coordination team welcomes you warmly

With nearly 25 years of clinical experience, our team has evolved into the specialists we are today. Our expertise includes study coordination, study conduct, medical documentation, data management, data analytics, medical IT, and electronic study platforms. Together, we have created the cvEDC system you access today, and we hope you will find it a clearly structured and intuitive platform.

Note that you can rely on the knowledge and experience of our team throughout the process of planning and conducting the study - should you have any questions, please feel free to contact us at any time; you will find our contact details in your profile data section after registration.

We are certified with ISO9001 quality management certificate and ISO27001 information security management certificate. All IT processes included in our cvEDC system are validated by a computer system validation procedure, which ensures data security and detailed recording of changes and access to our study data.

Our systems have been successfully validated many times by multiple independent investigators, CROs and sponsors in medical trials and drug approval studies.

Professional

Our employees are professional, knowledgeable, and motivated.

If you have any questions please contact us at any time. You will find our contact details after your registration in the section of your profile data.

Quality

We believe in the principle of quality and the importance of usability and excellent user experience with our products.

Please share your experiences with us and tell us which processes we can improve.

Reliability

Punctual and reliable delivery of the agreed products is one of our main goals.

Fast feedback for inquiries or problems is important to us and shapes a relationship based on mutual respect.

Legality

Our work abides by the strict legal confines of quality management and data protection regulations, including those of QM, ISO9001, CSV, GcP, GmP, GAMP, FDA CFR Part 11, ...