Results 261 to 270 of about 451,756 (297)
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investigational drug labelling

2009
The package of an investigational new drug intended for human use has to bear a label with a statement specific for the national regulations; EC: name and address of the company, identification of the substance or code, date of expiry/ retest, lot number, name of the responsible physician, to be used for clinical trials; US: “caution: new drug ...
openaire   +1 more source

LABELLING OF DRUGS

Medical Journal of Australia, 1972
openaire   +2 more sources

Recent Developments for the Deuterium and Tritium Labeling of Organic Molecules

Chemical Reviews, 2022
Sara Kopf, Florian Bourriquen, Wu Li
exaly  

Fine-tuning BERT for automatic ADME semantic labeling in FDA drug labeling to enhance product-specific guidance assessment

Journal of Biomedical Informatics, 2023
Yiwen Shi   +2 more
exaly  

Drug Trials Snapshots and Sexless Drug Labels

JAMA Internal Medicine, 2017
G Elliott, Cook, Erin E, Wilhelm
openaire   +2 more sources

Labeling and Single-Molecule Methods To Monitor G Protein-Coupled Receptor Dynamics

Chemical Reviews, 2017
He Tian   +2 more
exaly  

Labeling antineoplastic drugs

American Journal of Health-System Pharmacy, 1980
Mary E. Duafala, Scott Hulka
openaire   +1 more source

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