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Science / Validation / Good manufacturing practice / Verification and validation / Quality assurance / Packaging and labeling / Baddi / Cipla / Hygiene / Pharmaceutical industry / Business / Technology


Inspection Report for WHO
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Document Date: 2013-02-25 04:29:22

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File Size: 200,54 KB

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City

GENEVA / Bangalore / District Solan / Mumbai / /

Company

Dummy / Cipla Ltd / PERSONAL HYGIENE Personnel / /

Country

Switzerland / South Africa / Uganda / Ethiopia / India / /

Event

Product Issues / Product Recall / FDA Phase / /

Facility

Corporate Headquarters / Research Centre FPPs FPPs FPPs FPPs Research Centre The plant / The facility / /

IndustryTerm

manufacturing facility / validation protocol / defective products / natural products / manufacturing practices / culture media / manufacturing facilities / pharmaceutical products guideline / Manufacturing processes / food / media sterilization / production equipment / export products / Intermediate and bulk products / stainless steel loop / manufacturing areas / manufacturing / Laboratory equipment / Food grade oil / e.g. manufacturing / /

Movie

Standard Operating Procedure / On the job training / /

Organization

Drug Controlling Licensing Authority / World Health Organization / Drug Administration and Control Authority / Tanzania Food & Drugs Administration / Ageing Therapeutic Goods Administration Australia / National Drug Authority / Department of Health / Medicinal Control Council / /

/

Position

Poisons Board Secretariat General / Prime Minister / equipment and annual PM / Factory induction programmer / inspector / Summary General / General / logger / separate PM / Specific analyst / /

Product

Nevirapine tablets / Film Coated Tablets / Zidovudine tablets / validation / products / Lumefantrine Tablets / Hard Gelatin Capsules / Efavirenz Tablets / PRODUCT / National Drug / /

ProvinceOrState

Sikkim / Goa / Himachal Pradesh / /

Technology

API / validation protocol / /

URL

WWW.WHO.INT / /

SocialTag