Pharmacology and Toxicology
It is driven by chemistry but gradually directed by pharmacology and the clinical Sciences, drug research has contributed more to the development of medicine during the past century than any other scientific factor. Improving the science of drug development and instruction is important in fulfilling the public health. The initiation of molecular biology and, in particular, of genomic sciences is having a deep conclusion on drug discovery. Emphasis is positioned on the contrast between the academic and industrial research operating environments, which can influence the efficacy of research collaboration between the two communities, but which plays such an important role in drug innovation. The strategic challenges that research directors aspect are also emphasized. In discovery process comprises the early phases of research, which are designed to identify an investigational drug and achieve primary tests in the lab. This first stage of the process proceeds almost three to six years. By the end, investigators hope to identify a accomplished drug aspirant to further study in the lab and in animal models, and then in people. These advances offer great ability, but also add complexity to the R&D process. In order to ensure the safety and efficacy of personalized therapies that are used alongside diagnostics, clinical trial protocols must be modified and enhanced.
- Food Safety and Environmental Toxicology
- Toxicology Applications
- Environmental Pharmacology
- Pharmacological Testing
- Cardiovascular Pharmacology
- Applied Pharmacology
- Medical and Clinical Toxicology
- Toxicology Applications
- Forensic Toxicology
- Analytical Toxicology
- Cardiac Medications
- Medicine Development and Safety Testing
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Pharmacology and Toxicology Conference Speakers
Recommended Sessions
- Chemical and Pharmaceutical Engineering
- Drug Design And Development
- Drug Formulation Procedures
- Drug Product Manufacturing
- Biomarkers in Drug Design
- Clinical Trails & Biotherapeutics
- Computer Aided Drug Design (CADD)
- Drug Delivery and Distribution
- Entrepreneur Investment
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- Medicinal Chemistry and Drug Discovery Advancements
- Methodological Advancements in Pharmaceutical Industries
- Molecular Modelling in Drug Designing
- Novel Drug Delivery System
- Novel Drug Target Approaches
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- Pharmacokinetics and Pharmacodynamics
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- Traditional Medicine Design
- Types of Formulations
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- Regulatory Harmonization & Compliance - Biologics Meet 2026 (UK)
- Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Regulatory Science and Clinical Trial Innovations - Euro Antibiotics 2025 (Netherlands)
- Regulatory updates on Biosimilars - Eurobiosimilars 2026 (Italy)
- Rehabilitation and Physical Therapy in Pain - Pain Management 2026 (France)
- Risk-Based Monitoring and Trial Optimization - Clinical Trials-2026 (UK)
- Safety Pharmacology - Pharmacology 2026 (Italy)
- Safety Reporting in Early Phase Trials - Clinical Trials-2026 (UK)
- Semi-Solid Dosage Forms - Formulations 2025 (France)
- Sexually Transmitted Bacterial Infections and Resistance Trends - Euro Antibiotics 2025 (Netherlands)
- Signal Prioritization and Management Techniques - Clinical Trials-2026 (UK)
- Single-Use Technologies in Production - Biologics Meet 2026 (UK)
- Site Management Innovation - Clinical Research 2026 (UK)
- Smart Drug Delivery Systems - Formulations 2025 (France)
- Solid Dosage Forms - Formulations 2025 (France)
- Stem Cell and Genetic Clinical Research - Clinical Research 2026 (UK)
- Stewardship Programs in Human and Animal Health - Euro Antibiotics 2025 (Netherlands)
- Structure-Based Drug Design and Molecular Docking - Euro MedChem and CADD 2025 (France)
- Supply Chain Management - Pharmaceuticals-2025 (France)
- Sustainable Antibiotic Practices and Global Policy - Euro Antibiotics 2025 (Netherlands)
- Sustainable Biologics Manufacturing - Biologics Meet 2026 (UK)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Synthetic and Green Medicinal Chemistry - Euro MedChem and CADD 2025 (France)
- Systems Pharmacology and Drug Modeling - Euro Pharmacology 2025 (France)
- Target Identification and Validation - Euro MedChem and CADD 2025 (France)
- Targeted Drug Delivery and Nanomedicine in Infectious Diseases - Euro Antibiotics 2025 (Netherlands)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Role of CROs in Clinical Trial Execution - Clinical Trials-2026 (UK)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology - Pharmacology 2026 (Italy)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Germany)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Veterinary Pharmacology - Pharmacology-2025 (Germany)