Efficient, successful and high-quality project management is based on longstanding experience, reliable standards and excellent communication.
We at Forschungsdock GmbH are strong partners of our clients and fully identify with the projects and tasks we are commissioned with. We always keep the whole team in focus and offer an on time and on budget performance achieved via clear and target-oriented project management.
We manage phase I to IV clinical trials with medicinal products and studies with medical devices based on your or our SOPs, as feasible.
You plan to start the clinical development of a medicinal product or medical device and are in need of experienced, pragmatically thinking project managers? We support you and your plans.
In dependence of the size of your project we conduct your trial with our employees or cover "sponsor oversight" if commissioned by you. This means the steering and control of cooperation partners, e.g. in international studies or studies with a large number of investigational sites. If requested, we support you in the selection of cooperation partners and consult you with respect to study set-up.
The risk-based preparation and conduct of your study, the management of the study budget as well as continuous status updates for you as sponsor are part of our services.
We are happy to take on the generation of study-specific documents as e.g. clinical study protocol, project plan or monitoring manual / monitoring plan as well as the submission of the clinical trial applications to competent authorities and Ethics Committees.
We ensure the study's quality by continuous quality control starting with the selection of suitable investigational site up to study closure.
Use our experience and strength for the realisation of your projects!