We simplify the regulatory complexity you face when bringing your medical devices to local and global markets, with the support of our expert team. We provide end-to-end consulting throughout CE, MDR, FDA and TİTCK processes.
End-to-end consulting support throughout global certification processes such as CE Marking, MDR/IVDR and FDA.
Learn moreA seamless and complete entry process into the Turkish medical market through TİTCK and UMT compliance.
Learn moreDocument the safety of your device with MDR-compliant, scientifically grounded clinical evaluation reports.
Learn moreThe international movement of medical devices requires meticulous coordination in customs clearance, warehousing and distribution network management. At Şah Grup, we ensure your devices move safely and smoothly from source to end point, standing by you at every step of your supply chain.
End-to-end operational support in customs clearance, logistics planning and international distribution processes.
Learn moreThe right market research, the right investor matching and the right commercialization strategy form the foundation of sustainable growth. Şah Grup stands by medical technology companies as a trusted advisor in these three areas.
Get detailed information about market research, investor matching and commercialization consulting.
