It was a real pleasure to be part of Inventicon, held at Pride Plaza, Delhi, on 21st and 22nd August 2025. The event brought together leaders from the medical device regulatory domain, creating a strong platform for discussions on compliance, quality, and patient safety.
Panel Discussion on Evolving Device Regulations
I had the opportunity to be part of a panel discussion on:
“Evolving device regulations- Ensuring compliance, quality and patient safety.”
The discussion covered key themes such as:
- Essential principles of safety and effectiveness for medical devices and the role of standards
- Tools and strategies for quality improvement and patient safety
- Measures and benchmarks to achieve desired outcomes
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Moderator
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Mr. Parveen Jain, RAC (Devices), Senior Director, Quality and Regulatory Affairs Asia Pacific, Fresenius Medical Care
Panellists
- Mr. Bivash Chakraborty, Head – Regulatory Affairs & Quality & Public Business – India & South Asia, Biomerieux India Pvt. Ltd.
- Mr. Anil Chaudhari, Founder and CEO, Operon Strategist
- Ms. Jhankhana Gyani, Head – QRA, Draeger India
- Mr. Alok Kumar Soni, Head – Regulatory Affairs & Quality Assurance, India & South Asia, Bio-Rad Laboratories (India) Pvt. Ltd.
Key Takeaways from the Session
The session was attended by over 150 delegates from the regulatory domain, making the discussion highly engaging and impactful.
One of the important points I emphasized was the way gaps between design and manufacturing processes can sometimes weaken the product development chain. Such gaps may affect product efficacy and safety, leading to customer complaints or even product failures. Addressing these challenges through a strong regulatory framework and effective quality strategies is essential for achieving safe and reliable medical devices.
The session was well navigated by Mr. Parveen, and each panellist contributed meaningful perspectives that ensured attendees left with clear takeaways on navigating evolving regulations.
A Truly Enriching Experience
Inventicon 2025 was not just an event but an excellent opportunity to exchange knowledge, connect with industry experts, and reflect on how the medical device ecosystem can evolve with changing regulations.
At Operon Strategist, we remain committed to supporting manufacturers and startups in achieving compliance while ensuring quality and patient safety remain at the center of every decision.