Pure Global AI
LMHRA DOC-GDL-008

DOC-GDL-008 — printed document-control code

Guidelines on Inspectorate and Post-Market Surveillance (PMS)
LiberiaLiberia Medicines and Health Products Regulatory AuthorityGMP/QMSEffective 2026-04-16
Official source linked
What this code is

DOC-GDL-008 — printed document-control code is the official LMHRA identifier for “Guidelines on Inspectorate and Post-Market Surveillance (PMS)”. DOC-GDL-008 — printed document-control code is the official identifier LMHRA uses for this instrument.

Instrument
DOC-GDL-008
Full name
DOC-GDL-008 — printed document-control code
Category
GMP/QMS
Source links
Source publication
English
Open the source text
Linked source text; confirm the publisher, publication details and any later amendment or consolidated version.
Readable HTML
1 language version
Read the full text →
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
—
Effective
2026-04-16
Readable full text

Open a language version

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

English full textEnglish — original textRead HTML →
About this regulation

Guidelines on Inspectorate and Post-Market Surveillance (PMS)

Complete official 104-page LMHRA guideline with detailed medical-device GMP provisions covering design controls, quality systems, purchasing, traceability, process control, inspection and corrective measures, plus market surveillance and disposal. The document-control field states DOC-GDL-008, issue 13 April 2026, Version 01; cover and running headers instead show Version 003 and some headers DOC-GDL-018, 2025. Original inconsistencies are preserved.

DOC-GDL-008 — printed document-control code is the official identifier LMHRA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

Source linked