Synopsis
.- 1 Percutaneous Absorption
.- 2 Animal Models for Percutaneous Absorption
.- 3 Mitigating Dermal Exposure to Agrochemicals
.- 4 Importance of In Vitro Drug Release
.- 5 Diffusion Cell Design
.- 6 In Vitro Product Quality Tests and Product Performance Tests for Topical and Transdermal Drug Products
.- 7 Safety and efficacy testing of topical products; Practical considerations
.- 8 Challenges in Evaluating Bioequivalence of Topical Dermatological Drug Products
.- 9 Methods for the Assessment of Bioequivalence of Topical Dosage Forms: Correlations, Optimization Strategies and Innovative Approaches
.- 10 Application of Microdialysis in Assessing Cutaneous Bioavailability
.- 11 Follicular Drug Penetration
.- 12 Development of Pilosebaceous Unit-Targeted Drug Products
.- 13 Deep Percutaneous Penetration into Muscles and Joints: Update
.- 14 Efficacy & Toxicity of Microneedle based devices
.- 15 Mathematical Models for Topical and Transdermal Drug Products
.- 16 Transdermal Patches: An Industrial Perspective on the Relevance of in vitro Skin Permeation Studies and Approaches on Design of Manufacturing Processes
.- 17 Transdermal Drug Delivery Systems. Regulatory Considerations: NDA and ANDA Requirements
.- 18 Transdermal Estradiol and Testosterone Transfer in Man: Existence, Models, and Strategies for Prevention
.- 19 Effects of occlusion on dermal drug delivery: implications for bioequivalence measurement
.- 20 Challenges with Clinical Endpoints - Bioequivalence
.- 21 Clinical Considerations of Bioequivalence For Topical Dermatologic Drugs
.- 22 OECD Test Guideline 428 - A method for in vitro percutaneous absorption measurement?
.- 23 Bioequivalence, Quality, and Novel Assessment Technologies for Topical Products: Current Challenges and Future Prospects.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
