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Consultancy service in the scope of:
- strategic planning of research and development activities,
- risk identification and assessment,
- programme planning, organizing, monitoring and supervising of clinical research of medical products and devices,
- optimal selection of subcontractors,
- overseeing research and development project implementation,
- registration of medical products and devices,
- independent quality oversight,
- interpretation and implementation of procedures according to their local legal regulations,
- overseeing registration processes of investigational medical products and devices.
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