GUIDED offers hands-on support and consulting for many problems young companies and projects face when entering clinical research. Our expertise is to set-up high quality studies with small teams and virtual companies.

We know what is needed to become a sponsor, to prepare and conduct a clinical trial. We support you to select the right partners, investigators and CROs according to GCP. Together we draft your clincial development strategy and budget to apply for funding. We write and review study protocols, investigator brochures and other clinical documents.

We help you to bring your drug in suitable animal models and translate your research results into doable study protocols giving you meaningful results in the end. We develop, improve or challenge your quality management system to meet your organization's needs and authorities' expectations, helping you to survive inspections and due diligences. 

We will support you through all aspects of early development to large clinical trials. Along this way we can be your GUIDE, but we can also be your SHERPA carrying part of your load.