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Pharmaceutics / Quality / Artemether/lumefantrine / Pharmaceuticals policy / Validity / Validation / Good manufacturing practice / Artemether / Inspection / Pharmaceutical industry / Business / Technology


Prequalification of Medicines Programme
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Document Date: 2014-10-23 04:55:10


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City

GENEVA / Beijing / /

Company

The Beijing Novartis Pharma Ltd / Beijing Novartis Pharma Co. Ltd. / 14 WHO Public Inspection Report Beijing Novartis Pharma Ltd / Novartis Suffern USA / HP / 8 WHO Public Inspection Report Beijing Novartis Pharma Ltd / Beijing Novartis Pharma Ltd / /

Country

Switzerland / China / South Africa / /

/

Event

Product Issues / Business Partnership / Product Recall / FDA Phase / Reorganization / /

Facility

QC laboratory / Beijing Institute of Drug Control / Chemistry Laboratory The laboratory / HPLC Laboratory One laboratory / Beijing airport / /

IndustryTerm

technology department / quality control equipment / analytical equipment / web application / suitable equipment / cold chain products / Manufacturing areas / manufacturing science / manufacturing site / imported drug products / laboratory equipment / dissolution equipment / pharmaceutical products / Manufacturing processes / manufacturing process / /

MedicalCondition

deficiency / /

Organization

World Health Organization / ICH / US Federal Reserve / Manufacturer Unit / Beijing Institute of Drug Control / Kenya Authority / /

/

Position

head of compliance / contractor / General information Name / Summary General / V-model / GAM5 and company guidelines / Head of speciality unit and head of manufacturing science / /

Product

Product Quality Review Quality Risk Management Deviation control Change control Complaints / Coartem tablet / Coartem/Riamet / Artemether/Lumefantrine 20/120mg Tablets / Coartem tablets / PRODUCT / /

ProvinceOrState

Changping District / /

RadioStation

8 WHO / 14 WHO / /

Technology

X-ray / API / spectroscopy / Process validation Protocol / process control / /

URL

WWW.WHO.INT / /

SocialTag