CDSCO G.S.R.G.S.R. 729(E)
G.S.R. 729(E) is the official CDSCO identifier for “Medical Devices (Amendment) Rules, 2018”. G.S.R. 729(E) is the official identifier CDSCO uses for this instrument.
- Instrument
- G.S.R.
- Full name
- G.S.R. 729(E)
- Category
- Clinical Trials
- Authority source
- English
- Readable HTML
- 0 articles · 1 language version
- Published
- 1 August 2018
- Effective
- 1 August 2018
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Medical Devices (Amendment) Rules, 2018
G.S.R. 729(E) of 1 August 2018, the first amendment to the Medical Devices Rules, 2017. Inserts the requirement that an application for import or manufacture of an in-vitro diagnostic medical device be accompanied by a performance evaluation report as specified in the Fourth Schedule. Official gazette PDF ingested as corpus text.
G.S.R. 729(E) is the official identifier CDSCO uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.