Classification Of Medical Devices And The Regulatory Framework In India, Indonesia, And Thailand Seminar

In the second segment of our series, we explore the classification of medical devices and the regulatory landscape for manufacturers in India, Indonesia, and Thailand. Our focus is on comparing these regulations with those of established players such as the US, UK, and EU. We delve into the intricate classification systems employed by each country and the regulatory requirements manufacturers must navigate to ensure compliance. Through this analysis, we aim to illuminate the complexities of the regulatory frameworks, providing valuable insights for stakeholders in the healthcare industry. Be sure to stay tuned for a comparative analysis chart summarizing the key differences as we embark on this regulatory journey together.