Are you facing problems with Medical Device development  with a fragmented workflow relying on multiple service providers? CH-Regulate B.V provides a “one stop medical device product development service” from product conceptualization, design & development, all cellular, molecular, mechanical, histological, drug/growth factor coating and release profile analysis, prototype development, validation, technology transfer, and GMP manufacturing under ISO:13485 regulations for CE/FDA approval by a team of experts with 30+ years of experience in the field. Specifically, the team has in-depth expertise in dental, orthopedic, wound care, bone graft substitutes -derived from xenografts, allografts, bioactive ceramics, calcium phosphates, and composites.

See the services below offered by CH-Regulate's expert team