If you are looking for an expert partner to manage your clinical trial, we’re at your service. As a full-service CRO we support you on all levels and in every step of your clinical research project.
Our clinical trial documentation services help sponsors generate documents which meet (local) requirements and applicable guidelines.
To choose your site well, you need good knowledge of the requirements of your study on the one hand, and knowledge of different site characteristics on the other hand.
We support sponsors and investigators by identifying the stakeholders that need to be involved in the application reviewing process.
At the core of good clinical trial work is of course good project and site management. We provide you with a dedicated clinical project manager and make sure you keep oversight at all times.
genae provides clinical safety services, such as Safety Management, DSMB & CEC and adverse event management services.
Your trial may need more than on-site monitoring. We ensure the right balance of risk based, remote and/or on-site monitoring to guarantee protocol and regulatory compliance.