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药物发现,开发和制造 499条(本栏目收费,不能显示细节,电话13136136841)
CLEARANCE OF NANOPARTICLES
DURING CIRCULATION
15150
DRUG DELIVERY STRATEGIES FOR
COMBATING MULTIPLE DRUG
RESISTANCE
15182
INTRACELLULAR TRAFFICKING OF
NANOPARTICLES: IMPLICATIONS
FOR THERAPEUTIC EFFICACY OF
THE ENCAPSULATED DRUG
15202
TOXICOLOGICAL ASSESSMENT OF NANOMEDICINE
15222
BIODEGRADABLE NANOPARTICLES
10985
RECOMBINANT SACCHAROMYCES
CEREVISIAE AS NEW DRUG
DELIVERY SYSTEM TO GUT: IN VITRO
VALIDATION AND ORAL
FORMULATION
11015
NASAL DELIVERY OF PEPTIDE AND
NONPEPTIDE DRUGS
11041
NASAL POWDER DRUG DELIVERY
11101
AEROSOL DRUG DELIVERY
11133
OCULAR DRUG DELIVERY
11179
MICROEMULSIONS AS DRUG
DELIVERY SYSTEMS
11219
TRANSDERMAL DRUG DELIVERY
11243
VAGINAL DRUG DELIVERY
11259
PHARMACEUTICAL
PREFORMULATION:
PHYSICOCHEMICAL PROPERTIES OF
EXCIPIENTS AND POWDERS AND
TABLET CHARACTERIZATION
11329
ROLE OF PREFORMULATION IN
DEVELOPMENT OF SOLID
DOSAGE FORMS
11381
TABLET PRODUCTION SYSTEMS
11501
CONTROLLED RELEASE OF DRUGS
FROM TABLET COATINGS
11547
EFFECTS OF GRINDING IN
PHARMACEUTICAL TABLET
PRODUCTION
11613
ORAL EXTENDED - RELEASE
FORMULATIONS
11639
CYCLODEXTRIN - BASED
NANOMATERIALS IN
PHARMACEUTICAL FIELD
11671
NANOTECHNOLOGY IN
PHARMACEUTICAL
MANUFACTURING
11695
PHARMACEUTICAL
NANOSYSTEMS: MANUFACTURE,
CHARACTERIZATION, AND
SAFETY
11735
OIL - IN - WATER NANOSIZED
EMULSIONS: MEDICAL APPLICATIONS
117733
GOOD MANUFACTURING
PRACTICES ( GMP ) AND RELATED
FDA GUIDELINES
11813
ENFORCEMENT OF CURRENT GOOD
MANUFACTURING PRACTICES
11855
SCALE - UP AND POSTAPPROVAL
CHANGES (SUPAC) REGULATIONS
11877
SCALE - UP AND POSTAPPROVAL
CHANGES (SUPAC) REGULATIONS
11907
NATIONAL GMP REGULATIONS AND
CODES AND INTERNATIONAL GMP
GUIDES AND GUIDELINES:
CORRESPONDENCES AND
DIFFERENCES
11927