Join us on April 24th for an exclusive webinar hosted by Qualtech Consulting Corporation, where we’ll provide clear, practical insights into India’s medical device regulatory framework.
As India’s healthcare sector experiences rapid growth, it opens exciting opportunities for medical device companies. Yet, navigating the country’s evolving and often complex regulatory landscape can be challenging — especially for newcomers and even for experienced industry players.
This webinar will provide valuable insights into:
- India’s medical device regulatory framework and approval process
- Classification of medical devices (Class A–D) and key requirements
- Common challenges and best practices for faster registration
- Case studies to help you understand real-world approval timelines
Webinar Details
- Date: Thursday, April 24, 2025
- Time: 4PM (GMT +8) | 10AM (CET)
- Language: English
- Registration Link: https://forms.gle/pJMZ9vaazhDmQGq57
Gain valuable insights to navigate India’s regulatory framework with confidence. Reserve your spot today!
For enquiries, contact us at globalra@qualtechs.com.
We look forward to seeing you there!