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GOOD MANUFACTURING PRACTICE GUIDELINE FOR PHARMACEUTICAL PRODUCTS · DECfinder

USAID DEC

GOOD MANUFACTURING PRACTICE GUIDELINE FOR PHARMACEUTICAL PRODUCTS

Archived 2024DEC · Record PA-00M-RV7

USAID DEC

GOOD MANUFACTURING PRACTICE GUIDELINE FOR PHARMACEUTICAL PRODUCTS

PQM · 1970

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In this record

01Abstract
02Classification
03Related records

Record ID: PA-00M-RV7
Language: English
File: PDF
Contract no.: GHS-A-00-09-00003-00##AID-GHS-A-00-09-00003

Abstract

No abstract is available for this document.

Connected topics

Manufacturing903→
Pharmaceuticals571→

Related documents

Documents in this collection

Guideline for registration of medicines

USAID DEC

Guideline for registration of medicines

Ensuring the quality of medicines in low-income countries : an operational guide

USAID DEC

Ensuring the quality of medicines in low-income countries : an operational guide

Initial environmental examination

USAID DEC

Quality control

459→

Water supply engineering221→

Containers64→

Classification

Document type: Technical Guidance
DEC type: Handbook/Manual
Geography: AfricaEthiopia
Subject: Water supply engineering
DEC terms: ContainersCultures (biological)FiltersManufacturingPackaging
Language: English

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Initial environmental examination

Open record

National Quality Assurance Policy For Medicines and Other Health Product

USAID DEC

National Quality Assurance Policy For Medicines and Other Health Product

Manual for internal monitoring of fortified maize flour

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Manual for internal monitoring of fortified maize flour

A WHO guide to good [vaccine] manufacturing practice (GMP) requirements -- part 1 : standard operating procedures and master formulae

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A WHO guide to good [vaccine] manufacturing practice (GMP) requirements -- part 1 : standard operating procedures and master formulae

Pharmaceuticals

Pressure

Quality control