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TFDA 特定醫療器材專案核准製造及輸入辦法

特定醫療器材專案核准製造及輸入辦法

Regulations for Project Approval of Manufacture and Import of Specific Medical Devices
TaiwanTaiwan Food and Drug AdministrationClinical Trials
What this code is

特定醫療器材專案核准製造及輸入辦法 is the official TFDA identifier for “Regulations for Project Approval of Manufacture and Import of Specific Medical Devices”. 特定醫療器材專案核准製造及輸入辦法 is the official identifier TFDA uses for this instrument.

Instrument
特定醫療器材專案核准製造及輸入辦法
Full name
特定醫療器材專案核准製造及輸入辦法
Category
Clinical Trials
Source links
Authority source
Chinese
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Readable HTML
25 articles · 1 language version
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
April 22, 2021
Effective
Readable full text

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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

About this regulation

Regulations for Project Approval of Manufacture and Import of Specific Medical Devices

Authorized subordinate pcode L0030119, announced 22 April 2021. 25 articles. The Ministry of Justice English translation page returns empty bytes, so only the Chinese controlling text is ingested.

特定醫療器材專案核准製造及輸入辦法 is the official identifier TFDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.