IVDR webinar series
Navigating IVDR for Indian manufacturers with proven notified body support
India’s IVD sector is evolving fast, with stricter Central Drugs Standard Control Organisation (CDSCO) requirements and growing pressure to meet EU IVDR standards for global market access. Only a handful of Indian manufacturers have secured IVDR certification so far making it crucial to understand the new classification rules, regulatory pathways, and compliance expectations.
Join our 2-part IVDR webinar series, where our experts will share key insights on IVDR classification and conformity assessment routes, the preparation of technical documentation and clinical evidence. You will also hear how DNV, as a Notified Body, supports Indian manufacturers in achieving IVDR certification with confidence.
Who should attend:
- IVD manufacturers and exporters targeting the European market
- Regulatory Affairs (RA) and Quality Assurance (QA) professionals
- Business leaders in the medical device and diagnostics sector
- Compliance, certification, and market access specialists
- Clinical and technical documentation specialists
Register below