Regulatory Affairs Specialist

Future Medical Supply Co., Ltd.

Nonthaburi, Mueang Nonthaburi District, Nonthaburi

• Investigating whether the Health Product is a medical device requiring registration with MOH, determining its risk classification and its route of submission.
• Liaise with suppliers to obtain registration documents.
• Preparing and submitting documents related to Initial, Renewal, Variations/Change Notification of medical devices and various licenses, follow-up until approval process.
• Maintain regulatory database for the Company.
• Liaising with government agenciesl and external organizations on matters relating to medical device regulatory requirements.
• Preparation of regulatory report to the relavant Geovernment agencies. More Detail

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