công ty TNHH andaman medical việt nam

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With a global experience in medical devices regulatory, compliance and clinical affairs, Andaman Medical is trusted partner across Southeast Asia. Strategically positioned throughout Southeast Asia - Singapore, Malaysia, Indonesia, Philippines, Thailand and Vietnam), we facilitate manufacturers from USA, Canada, Europe, ANZ, Japan, Korea, China to reach the ASEAN market and beyond, focusing on intricate regulatory differences between global regulations and diligently following local procedures and updates. Andaman Medical services for Medical Devices and Healthcare include: - Regulatory Intelligence - Clinical Evaluation - Product Registration & Establishment Licensing - Quality Management Systems (ISO 13485, US FDA 21 CFR part 820, GDPMD) - Business Services - Auditing, Training & Support Andaman Medical provides a complete range of services for all Quality, Regulatory and Clinical needs for South East Asia submissions. Our methodology brings time and financial efficiency for compliance-related issues with regulatory requirements. In addition to stream-lining your submission process, we offer expert training in all phases of the development and regulatory process. We are always looking for bright, energetic people who would like to advance their career in the medical device regulatory industry

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