From Concept to Compliance: Mastering Medical Device Clinical Studies
Thursday, October 9th, 2025 @ 3:00 PM IST
Webinar Registration has been closed.
Top Reasons to attend this webinar.
Gain Expert Knowledge on Clinical Investigation for Medical Devices
Learn to Design Compliant Clinical Investigation
Practical Insights Through Case Studies
Interactive Q&A Session with Dr. Ashwini and Subject Experts
Understand Regulatory Frameworks in India and Globally – Clarifies complexities of MDR 2017, ISO 14155, CDSCO, FDA regulations, and how to navigate them effectively.
Who should attend this webinar
- Medical device manufacturers and innovators
- Clinical research professionals
- Regulatory affairs specialists
- Startups in medtech
- Quality assurance teams
- Healthcare professionals interested in device development
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Connect with us for an insightful webinar on mastering medical device clinical studies—and gain expert guidance on compliance, trial design, and global regulatory frameworks.
In this Upcoming webinar, Master Medical Device Clinical Studies with our Experts
Dr. Ashwini Kumar
Founder & CEO
Rajiv Kanwal
Assistant Manager | BD
Nitesh Grover
Project Manager
Frequently Asked Questions
Who should attend this webinar?
Who should attend this webinar?
This webinar is ideal for:
- Medical device manufacturers and innovators
- Clinical research professionals
- Regulatory affairs specialists
- Startups in medtech
- Quality assurance teams
- Healthcare professionals interested in device development
What will I learn from this session?
What will I learn from this session?
You’ll gain:
- A complete overview of clinical study requirements for medical devices
- Insights into MDR 2017 and ISO 14155:2020 compliance
- The differences between pilot and pivotal studies
- Key documentation and regulatory strategies for faster approvals
- Real-world case studies demonstrating successful trials and approvals
Is this webinar applicable to global regulations or only India?
Is this webinar applicable to global regulations or only India?
While the webinar emphasizes Indian regulations (MDR 2017, CDSCO), it also touches on global frameworks including FDA, EU MDR, ISO 14155, and ICH GCP—making it relevant for international participants.
Will I receive a certificate of participation?
Will I receive a certificate of participation?
Yes, attendees will receive an e-certificate of participation after the webinar.
Is there any cost to attend the webinar?
Is there any cost to attend the webinar?
No, this webinar is completely free of charge.
Will a recording be available after the session?
Will a recording be available after the session?
Yes, registered participants will receive access to the webinar recording and presentation slides via email.
Can I ask questions during the webinar?
Can I ask questions during the webinar?
Absolutely! There will be a dedicated Q&A session at the end where speakers will address audience questions live.
How do I register for the webinar?
How do I register for the webinar?
Click the Register Now button on this page and fill out the short registration form to reserve your spot.
