Dantech Dental Lab Participated in CDSCO–CII Workshop on Medical Devices Regulations
Dantech Dental Lab participated in the CDSCO–CII One-Day Workshop on Medical Devices Regulations, held on 30 June 2026 at Greater Noida.
Representing Dantech, Mr. Mukesh, QARA Representative, attended the workshop to gain valuable regulatory insights and strengthen our understanding of India’s evolving medical device regulatory framework.
Organized by the Central Drugs Standard Control Organization (CDSCO) in collaboration with the Confederation of Indian Industry (CII), the workshop focused on the key changes in India’s medical device regulatory framework. The sessions covered key topics including licensing procedures, retention of the license, post-approval change management, clinical evaluation & investigation, substantial equivalence approach, quality management expectations, and post-market surveillance.
One of the key highlights of the workshop was the opportunity to interact directly with CDSCO officials and discuss the evolving Indian regulatory approach for dental prosthesis. These discussions provided practical clarification on regulatory expectations, implementation challenges, and compliance requirements, enabling organizations to better navigate the evolving regulatory environment.
By participating in this workshop, Dantech continues to reinforce its commitment to regulatory excellence, quality, and patient safety. The knowledge gained will support our ongoing and upcoming regulatory initiatives, ensuring that our medical devices and processes remain aligned with the Medical Devices Rules (MDR), 2017.
At Dantech, we believe that continuous learning and proactive engagement with regulatory authorities are essential to delivering safe, compliant, and high-quality prosthetic solutions. We remain committed to staying at the forefront of regulatory developments while maintaining the highest standards of quality and compliance.
Participation in industry-led regulatory workshops such as the CDSCO–CII One-Day Workshop on Medical Devices Regulations enables Dantech to stay informed about the latest regulatory expectations and industry best practices. These valuable insights strengthen our quality systems and support our mission of delivering innovative, compliant, and patient-centric dental prosthetic solutions.
