Re: Classes of medical devices or medical devices for which manufacturers or importers are required to obtain a license, B.E. 2563 (2020)
Re: Rules, procedures and conditions for preparation of reports on medical device malfunctions or adverse events occurring to consumers and reports on field safety corrective actions for medical devices, B.E. 2563 (2020)
Notification of the Ministry of Public Health (No.232) B.E. 2544 (2001) Re: Repeal of the Notification of the Ministry of Public Health (No.14) B.E. 2522 (1979)
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