Back to Results
First PageMeta Content
Science / Validation / Good manufacturing practice / Quality management system / Quality assurance / Packaging and labeling / Pipe / Adolphe Appia / Pharmaceutical industry / Business / Technology


Prequalification of Medicines Programme
Add to Reading List

Document Date: 2013-03-22 05:49:16


Open Document

File Size: 300,60 KB

Share Result on Facebook

City

Geneva / Shanghai / /

Company

Page / APIs Laboratory / Manufacturer Zhejiang Hisun Pharmaceutical Co. Ltd. / Zhejiang Hisun Pharmaceutical Co. Ltd. / /

Country

Switzerland / /

/

Event

Business Partnership / FDA Phase / /

Facility

QC laboratory / LABORATORY CONTROLS QC / Production facility / Hangzhou airport / /

IndustryTerm

cell bank / exhaust systems / veterinary products / test equipment / validation protocol / manufacturing practices / manufacturing areas / manufacturing facilities / written validation protocol / active pharmaceutical ingredients / chemical / ancillary systems / equipment management / food / manufacturing process / /

Organization

World Health Organization / MHRA / Belarus Authority / FDA / German Authority / www.who.int Laboratory / /

/

Position

General information Name / correspondent / Summary General / MATERIALS MANAGEMENT General / QA Manager / /

Product

CH-1211 Geneva / concentrate / /

ProvinceOrState

Zhejiang Province / /

PublishedMedium

construction Equipment / /

RadioStation

11 WHO / /

Technology

API / written validation protocol / /

URL

www.who.int / /

SocialTag