Medical device industry seminar in emerging countries Part 2

In Part 2 of our series, we delve into the classification of medical devices and the regulatory landscape for manufacturers in India, Indonesia, and Thailand, comparing them with established players like the US, UK, and EU. We explore the intricate classification systems each country employs and the regulatory requirements manufacturers must navigate for compliance. By drawing parallels and distinctions, we shed light on the complexities of the regulatory frameworks, offering insights crucial for stakeholders in the healthcare industry. Stay tuned for a comparative analysis chart summarizing the key differences, as we embark on this regulatory journey together.
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