Confidentiality and protection of your information

We know that trust and confidentiality are essential in clinical research. Therefore, we treat all documents provided to us with the utmost confidentiality.

How does the process work?
As soon as you send us copies of your documents - be it:
the study protocol (synopsis)
the information sheet for patients
personal data
or further information on the study project

... these will be carefully checked by our team. They do not necessarily have to be final versions, drafts are also welcome. 

1️⃣ Analysis & risk assessment:
Our experts read, analyze and make an initial risk assessment.

2️⃣ Review by leading insurers:
The relevant information is summarized and forwarded to first-class insurance companies. These companies have experienced underwriting teams with in-depth knowledge of the pharmaceutical industry, medical device manufacturers and contract research organizations.

3️⃣ Risk assessment & quotation:
In close consultation with us, the insurers assess the risks of the clinical trial and calculate the insurance premium. This results in an individual offer for your desired insurance cover. If necessary, reinsurance is also initiated by the primary insurer.

Maximum confidentiality - guaranteed!

All parties involved are obliged to treat your information as strictly confidential. Confidentiality is a fundamental part of our business and is observed as standard in the insurance industry.

If desired, we can also record this in writing in a mutual non-disclosure agreement (NDA).

Do you have any questions? Contact us - we will be happy to advise you!

Your sensitive data is in safe hands with us - confidentiality is our top priority!