Source:http://linkedlifedata.com/resource/pubmed/id/10317216
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1982-8-14
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
H
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0160-6379
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
5
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
10-21
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:10317216-Drug Packaging,
pubmed-meshheading:10317216-Evaluation Studies as Topic,
pubmed-meshheading:10317216-Pharmaceutical Preparations,
pubmed-meshheading:10317216-Quality Control,
pubmed-meshheading:10317216-United States,
pubmed-meshheading:10317216-United States Food and Drug Administration
|
pubmed:year |
1982
|
pubmed:articleTitle |
Regulation of drugs for human use: FDA in action.
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pubmed:publicationType |
Journal Article
|