Back to Results
First PageMeta Content
Science / Pharmaceuticals policy / Pharmaceutical sciences / Measurement / Tests / Validation / Verification and validation / Quality assurance / Good manufacturing practice / Pharmaceutical industry / Validity / Food safety


© World Health Organization WHO Technical Report Series, No. 957, 2010 Annex 1 WHO good practices for pharmaceutical quality control laboratories
Add to Reading List

Document Date: 2010-06-15 08:55:52


Open Document

File Size: 437,14 KB

Share Result on Facebook

Company

QAS / /

Facility

The laboratory / /

IndustryTerm

pharmaceutical quality control laboratory / appropriate infrastructure / biological products / pharmaceutical substances / pharmaceutical excipient / pharmaceutical microbiology laboratories / pharmaceutical product / pharmaceuticals / pharmaceutical quality control laboratories / pharmaceutical excipients / analytical equipment / active pharmaceutical ingredient / pharmaceutical dosage form / specified chemical / blood products / inspection services / Data-processing equipment / chemical substance / governmental pharmaceutical quality control laboratory / manufacturing practices / chemical reference substances / pharmaceutical control laboratories / pharmaceutical product identification / pharmaceutical legislation / active pharmaceutical ingredients / agreed suppliers / energy supply / pharmaceutical products / e-records / /

MedicalCondition

disease / /

Organization

World Health Organization / WHO Expert Committee / national medicines regulatory authority / national pharmaceutical quality control laboratory / /

Position

quality manager / General / /

RadioStation

1 WHO / /

Technology

API / /

SocialTag