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Medical Device Regulatory Application Support Service

We will resolve the "impossible" in that drug application. Leave the response to pharmaceutical regulations to us.

Our company supports the introduction of medical devices, active pharmaceutical ingredients, and new food additives into the domestic market through a wide range of services, including drug application services, clinical trials, designated marketing authorization holders (DMAH), MF registration applications, and domestic representative services. Our representatives possess not only scientific knowledge but also high English proficiency and communication skills in their specialized fields. Additionally, we prepare appropriate workflows according to our clients' objectives, providing speedy and high-precision solutions. 【Features】 ■ Services including consulting ■ Support for PMDA consultations ■ Overseas support in English ■ Strict adherence to deadlines ■ Support for safety and quality operations *For more details, please download the PDF or feel free to contact us.

  • Welfare and medical equipment
  • Manual Creation

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