We are working with experts in all development stages. Our standard collaborations include:
- Specialized accredited laboratories
- Regulatory experts for the preparation and submission of registration dossiers of pharmaceutical products and technical files for medical devices
- IP experts for IP clearance and for the preparation and submission of our patent applications connected with our developments
- CRO’s for the preparation of clinical trial protocols and monitoring of all clinical studies
- Contract manufacturers for the production of our products during development stage and product supply after MA grant.
All our partners are well educated and highly skilled experts in their fields, who support us during development and are closely working with us during the whole journey until registration and marketing.