Challenges in Drug Design and Development
Animal models generally cannot recapitulate a totally disorder or disease. Challenges connected to heterogeneity of the patient population energy are reduce with increased clinical phenotyping and endotyping. Greater emphasis on human data power lead to improved target identification and validation
- Computer-Aided Drug Design
- Rational Drug Design Approach
- Novel Approach
- Topical Drug Development
- Genetics in Drug Development
Related Conference of Challenges in Drug Design and Development
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&
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Challenges in Drug Design and Development Conference Speakers
Shanghai Institute for Biomedical and Pharmaceutical Technologies, China
Title:Exploring the relevance and considerations of implementing alternative approaches to the assessment of reproductive and developmental toxicity of pharmaceuticals under ICH S5(R3)
Shanghai Institute for Biomedical and Pharmaceutical Technologies, China
Title:Advances in prostate pharmacology and toxicology and cutting-edge developments in drug research
Industrial University of Santander, Colombia
Title: An Experimental Rat Model For The Evaluation Of Levofloxacin-induced Nociceptive Alterations And Protective Alternatives
Ganpat University, India
Title:Intranasal voriconazole-loaded nanoemulsion for enhanced therapy of cryptococcal meningitis
Shahid Beheshti University, Iran
Title:A randomized clinical trial study about using oral clonidine premedication in patients with jaw skeletal discrepancy undergoing bimaxillary orthognathic surgery about hemodynamic status and bleeding
Chungnam National University, South Korea
Title:Rubianol B isolated from Rubia philippinesis induces RIP1/RIPK3-dependentg necroptosis in human colorectal cancer cells
IQVIA, United Kingdom
Title:Global drug development - Current trends, challenges and opportunities
Superior University, Pakistan
Title:Anti-oxidant and anti-inflammatory potential of Cichorium intybus
Z7 Biotech Ltd, United Kingdom
Title:Biophysics without protein purification: Tools to characterise drug action at GPCRs
Recommended Sessions
- BA/BE studies of Biologics and Biosimilars
- BCS & IVIVC Based Bio waivers
- Bioavailability
- Bioequivalence
- Bioequivalence Protocols: In vivo/ In vitro studies
- Biosimilars
- Challenges in Drug Design and Development
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- Drug Metabolism
- Drug Safety
- Factors Affecting Bioavailability
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- Recent approaches to Biosimilars
- Regulatory Requirements for Bioequivalence
- Significance of BA/BE Studies
- Study Designs
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