Strategical planning of different product developments in the field of Regenerative Medicine.
We offer our regulative know-how, our experience, and our network for the formulation of your strategy of your approach.

Planning and preparation of a multi-centric Phase III trial in the field of stem cell therapy, including the acquisition of necessary authorisations.
We offer our help with the planning and preparation of all necessary documents for the clinical studies, contacts to authorities, and the implementation in the trial sites.

Development of an electronic documentation system for clinical studies (e-CRF) with special emphasis on the requirements in Regenerative Medicine in cooperation with our partner D-Trust.
Together with our partner we create the e-CRF for your study and implement the system in your trial sites and we train your staff.

Building up clinical trial sites.
We support you in the implementation of your studies both regarding the close cooperation with the manufacturer as well as with the acquisition of the necessary documents for removal etc.