Healthium Medtech Limited
Siddhartha C. is an accomplished Director of Product Management at Microsoft, focused on developing Generative AI for the U.S. Federal sector since May 2016, and has received the Fast Company’s World Changing Idea Award. Previously served in multiple roles including Senior PMM, where contributions included the creation of a mosquito-gobbling machine for disease detection and the establishment of AI for Health, securing significant investment for health technology initiatives. Siddhartha C. has extensive experience as a Senior Manager collaborating with tech startups and the NHS to advance AI in healthcare and has a background as a Technology Evangelist involved in datacenter development. Currently, Siddhartha C. holds positions as an Investment Partner at rpv and an Advisor at Loyal VC, with past entrepreneurial experience as a co-founder of Tathaastu Healthcare Initiative. Educational credentials include an MBA from INSEAD, a Bachelor of Science in Computer Science from Birla Institute of Technology and Science, Pilani, a certification in Entrepreneurship from MIT, and a Bachelor of Technology in Computer Sciences and Engineering from Amity University.
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Healthium Medtech Limited
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Healthium Medtech Limited is a global medical devices company focused on products used in surgical, post-surgical and chronic care. Fuelled by its vision to provide “Access to precision medtech for every patient, globally," it is present across 80 countries. 1 in 5 surgeries conducted globally, uses a Healthium product . As of Fiscal Year 2021, Healthium Medtech is the largest independent medical devices company in India and 2nd largest in the surgical consumables market, the largest non-captive surgical needles manufacturer globally by volume . Healthium is driving Innovation by focusing on R & D. Since fiscal year 2018, it has sold 30 new products. It holds 85+ patents (including pending applications) in U.S, Europe and India. It has 7 high precision, integrated manufacturing facilities with global certifications like US FDA, TGA, ISO and CE under the stringent new EUMDR norms.