LMHRA DOC-GDL-016,DOC-GDL-016, Version 01
DOC-GDL-016, Version 01 is the official LMHRA identifier for “Guidelines for Emergency Use Authorization of Medical Products”. DOC-GDL-016, Version 01 is the official identifier LMHRA uses for this instrument.
- Instrument
- DOC-GDL-016,
- Full name
- DOC-GDL-016, Version 01
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- Registration
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Guidelines for Emergency Use Authorization of Medical Products
Complete official 31-page LMHRA guideline explicitly covering medical devices and diagnostics, including evidence requirements, conditions and annexes. The printed issue date is 13 April 2026 but implementation date is 16 April 2025, and its legal-basis text cites Public Health Act 2012, Act 851. These internal inconsistencies remain visible; no corrected commencement date or independently verified Liberian statutory basis is asserted.
DOC-GDL-016, Version 01 is the official identifier LMHRA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.