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Health / Pharmaceuticals policy / Drugs / Clinical pharmacology / Australia New Zealand Therapeutic Products Authority / Therapeutic Goods Administration / Medical prescription / Package insert / Prescription medication / Medicine / Pharmacology / Pharmaceutical sciences


DRAFT LABELLING REQUIREMENTS FOR MEDICINES UNDER THE AUSTRALIA NEW ZEALAND THERAPEUTIC PRODUCTS AUTHORITY Report on stakeholder consultation and consideration by the Joint Expert Committee on Trans Tasman Labelling Requi
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Document Date: 2014-07-18 01:53:13

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File Size: 238,06 KB

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City

Auckland / Sydney / /

Country

Australia / United Kingdom / New Zealand / /

Facility

BAR CODING / /

IndustryTerm

plasma products / biological products / blood products / low volume products / retail organisations / ophthalmic and topical medicinal products / healthcare providers / medicinal products / strength products / /

Organization

Therapeutic Goods Administration / Australia New Zealand Therapeutic Products Authority / Joint Australia New Zealand Therapeutic Products Agency / Joint Expert Committee on Trans Tasman Labelling Requirements for Medicines / /

Position

pharmacist / physician / Major / representative / General / Director a draft Managing / /

ProgrammingLanguage

EC / /

PublishedMedium

the Australia Prescription Products Guide / MIMS Annual / /

URL

http /

SocialTag