Unlock the Potential of the Indian Market
India represents one of the world’s fastest-growing and most dynamic economies, offering significant opportunities for manufacturers and exporters. However, market entry requires strict compliance with national regulatory authorities, including CDSCO for medical devices and BIS for product standards. As the international division of Quality Management Services India, QM Service Global combines global regulatory expertise with strong local technical knowledge to ensure seamless compliance and successful market access across India.
CDSCO Registration & Licensing Support
We provide complete assistance for CDSCO medical device registration, including Import License (MD-14) and Manufacturing Licenses (MD-5 / MD-9). Our team manages regulatory classification, documentation preparation, application filing, and authority coordination to ensure timely approval and regulatory compliance.
BIS Certification & ISI Marking
For products requiring mandatory Indian standards compliance, we offer full support for BIS Certification, including ISI marking and the Foreign Manufacturers Certification Scheme (FMCS). We guide you through application submission, factory inspection readiness, and compliance documentation.
Authorized Representation & Testing Coordination
Foreign manufacturers entering India must appoint an Indian Authorized Agent. We act as your official representative, handling regulatory communication and compliance obligations. Additionally, we coordinate product testing with NABL-accredited laboratories to ensure accurate and recognized test reports.
