Select your language

  • Document Management for Clinical Investigations

Our document management services provide comprehensive support in creating and structuring all essential clinical documents. We ensure your documentation is always complete and correct to meet regulatory authorities' requirements. With our many years of experience dealing with ethics commissions and authorities and our in-depth understanding of regulatory requirements, we offer you the benefit of a reliable partner for seamless document management.

Rely on our comprehensive service to expertly manage your clinical documents while ensuring strict compliance with industry regulations.

Our Services

Creation and maintenance of the Trial Master File

Essential document preparation

Essential document review

Technical File review

Submission dossier creation

Submission to IECs (independent ethics committees) and/or HA (health authorities)

How Can We Help You?

Take advantage of our expertise and work with us to make your clinical study successful.
Contact us today to find out more about how we can help you.

Bernhard Bichsel

Bernhard Bichsel

Co-CEO
Julie Tantau

Julie Tantau

Head of Clinical Operations

Contact us

Complete the short form below and we’ll get back to you as soon as possible.
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.