An awareness & hands-on workshop series designed for students, researchers, startup founders, & industry members to explore the Medical Devices & IVDs Ecosystem
Starting Up: Incorporation & DPIIT Recognition for MedTech (Virtual)
Protecting Innovation: Intellectual Property Rights (Virtual)
Product Design & Manufacturing (In Person) with an immersion at a leading Medical Device Industry
Regulatory – Hands-on workshop (In person) with an immersion at a leading Medical Device Industry
Clinical Validation (In Person) with an Immersion at a Hospital
Industry Immersion Partners
Clinical Immersion Partners
Intervention 1 - Starting Up: Incorporation & DPIIT Recognition for MedTech
Kickstart your MedTech entrepreneurial journey with a deep dive into the foundational steps of starting up.
This session will guide participants through the process of company incorporation, understanding different business structures, and the benefits of obtaining DPIIT Startup Recognition and Learn how to position your venture for success and leverage government initiatives, funding support, and startup-friendly policies tailored for innovators in the healthcare and medical device sectors.
Key Takeaways:
- Steps for company incorporation and choosing the right structure
- Understanding DPIIT Startup Recognition and its benefits
- Accessing government schemes and funding opportunities
- Legal and compliance aspects for MedTech startups
Date of the session - 30th October 2025 (Virtual Session) - 11:00 am to 01:00 pm
Duration - 2 Hours
Program fee - Nil
Intervention 2 - Protecting Innovation: Intellectual Property Rights
This session demystifies the essentials of Intellectual Property Rights (IPR) for innovators, startups, and researchers.
Gain insights into how to safeguard your innovations through patents, trademarks, and design registrations, and understand how IP protection strengthens your startup’s valuation, partnerships, and market edge.
Key Takeaways:
- Introduction to patents, trademarks, and design rights in MedTech
- Understanding the IP filing process and timelines
- Strategies for protecting innovations early in development
- Leveraging IP for collaborations, funding, and commercialization
Date of the session - 31st October 2025 (Virtual Session) -11:00 am to 01:00 pm
Duration - 2 Hours
Program fee - Nil
Intervention 3 - Product Design & Manufacturing: From Concept to Prototype (In-Person)
Bridge the gap between innovation and production through this immersive session conducted at leading Medical Device Industries
Participants will learn the fundamentals of medical device design, material selection, prototyping, and scaling up for manufacturing — while understanding the importance of quality standards and industrial design thinking in product development.
Key Takeaways:
- Introduction to design and product development stages
- Prototype development and design validation
- Manufacturing processes, supply chain, and quality management systems
- Industry visit for hands-on understanding of production workflows at leading Industries in Medical Devices Park, Sultanpur
Date of the session - 6th November 2025
Program fee - Registration is mandatory to share the payment link and confirm the participation.
- Student / Researcher (Per person) – 10 Participants - INR 1,000
- Start-up (Per Person) – 20 Participants - INR 3,000
- MSME/SME (Per Person) – 10 Participants - INR 5,000
Intervention 4 - Regulatory Pathways: Hands-on Workshop & Industry Immersion (In-Person)
Navigate the complex regulatory landscape of medical devices and IVDs with expert-led sessions and on-ground exposure at a leading MedTech manufacturing facility.
Participants will gain clarity on India’s regulatory framework, device classifications, documentation requirements, and pathways for product approval and certification.
Key Takeaways:
- Overview of Indian and global regulatory frameworks (CDSCO, ISO, CE, FDA basics)
- Device classification and registration process
- Understanding clinical evaluation and documentation requirements
- Hands-on exposure to regulatory compliance practices at an industry site
Date of the session - 5th November 2025
Program fee - Registration is mandatory to share the payment link and confirm the participation.
- Student / Researcher (Per Person) – 10 Participants - INR 1,000
- Start-up (Per Person) – 20 Participants - INR 3,000
- MSME/SME (Per Person) – 10 Participants - INR 5,000
Intervention 5 - Clinical Validation: Bridging Innovation and Evidence (In-Person)
Clinical validation is the bridge between innovation and patient impact.
This session, hosted at a leading hospital, will help participants understand the process of planning and executing clinical validation studies, documentation requirements, and ethical considerations for medical devices and IVDs.
Key Takeaways:
- Study design and data collection for medical devices
- Procurement Processes
- Insights from clinicians and industry experts during the hospital immersion
Date of the session - 5th November 2025
Program fee - Registration is mandatory to share the payment link and confirm the participation.
- Student / Researcher (Per Person) – 10 Participants - INR 1,000
- Start-up (Per Person) – 10 Participants - INR 3,000
- MSME/SME (Per Person) – 10 Participants - INR 5,000