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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)
An Introduction to Toxicogenomics
4477
Role of Bioactivation Reactions in
Chemically Induced Nephrotoxicity
4501
Drug Metabolism in Regulatory
Guidances, Clinical Trials, and
Product Labeling
4523
Drug Development
Process and Global
Pharmaceutical
Marketplace
4739
Regulation of Human
Pharmaceutical Safety
4757
Prior Art and Its
Use in Safety
Assessment Process
4827
Screens in Safety and
Hazard Assessment
4841
Formulations, Routes, and
Dosage Design
4859
Single - Dose (Acute) and
Pilot ( DRF ) Toxicity
Testing in Drug Safety
Evaluation
4923
Repeat - Dose Toxicity
Studies
5042
Immunotoxicology in
Drug Development
5064
Nonrodent Animal
Studies
5138
Developmental
and Reproductive
Toxicity Testing
5179
Carcinogenicity Studies
5219
Histopathology in
Nonclinical
Pharmaceutical Safety
Assessment
5258
Irritation and Local
Tissue Tolerance in
Pharmaceutical Safety
Assessment
5269
Pharmacokinetics and
Toxicokinetics in Drug
Safety Evaluation
5306
Special Concerns for
Preclinical Evaluation of
Biotechnology Products
5382
Safety Assessment of
Inhalant and Dermal
Route Drugs
5426
Special - Case Products:
Imaging Agents and
Oncology Drugs
5463
Occupational Toxicology
in Pharmaceutical
Industry
5475
Strategy and Phasing for
Nonclinical Drug Safety
Evaluation in Discovery
and Development of
Pharmaceuticals
5497
Application of In Vitro
Techniques in Drug
Safety Assessment
5526
Evaluation of Human
Tolerance and Safety in
Clinical Trials: FIM Trials
and Beyond
5599
Postmarketing Safety
Evaluation: Monitoring,
Assessing, and
Reporting of Adverse
Drug Responses
5673
Statistics in
Pharmaceutical
Safety Assessment
5710
Combination Products:
Drugs and Devices
5821
Qualifi cation of
Impurities, Degradants,
Residual Solvents,
and Leachables
in Pharmaceuticals
5838