[Technical Seminar] Medical Device and Healthcare Business Development and Regulatory Compliance Strategies
Learn from over 500 consultation achievements: Regulatory affairs and QMS during new market entry, development processes, exit strategies, and common pitfalls.
This seminar will explain the development and entry processes specific to regulated industries that are required for new entrants in the medical and healthcare fields. Taking into account the risks of setbacks due to insufficient understanding of regulations and deficiencies in the application of QMS in the early stages of development, we will systematically explain practical know-how to avoid "pitfalls" during entry, based on our experience of consulting over 500 companies and on-site practices. This includes an overview of business permits, QMS, commercialization, schedule design considering regulatory classifications, exit strategies from the development stage, and the utilization of public support. *For more details, please check the related links or the seminar details in the catalog.
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<Event Information> Format: Online lecture via Zoom Date and Time: November 24, 2026 (Tuesday) 13:30 - 14:30 Participation Fee: Free Instructor: Kazuko Shida, Instructor
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<Seminar Program (Tentative)> Chapter 1: Prerequisites for Medical Device Commercialization: The Reality of "Regulated Industries" You Should Know Chapter 2: Overview of Medical Device and Healthcare Commercialization and Common Pitfalls Chapter 3: Actions to Seize Winning Strategies
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We support Japan's "monozukuri" (manufacturing) with reliable services ranging from patent research and other intellectual property business solutions to technical translation services and intellectual property/engineer education. We offer high-quality services backed by over 40 years of experience at reasonable prices.
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