Advances In Bioavailability
In pharmacology, bioavailability BA is a subcategory of ingestion and is the part of a managed measurement of unaltered medication that achieves the systemic flow, one of the important pharmacokinetic properties of medications.
The overall emerging markets for therapeutic drugs totalled $131.4 billion in 2009. These regions include Latin America, China, Eastern Europe, the Middle East, South Korea, India, Russia, and South Africa. These regions are estimated at $145.8 billion in 2010 and expected to continue aggressive growth through 2015, reaching a figure of $214.2 billion, yielding a compound annual growth rate (CAGR) of 8% from 2010 to 2015.
- Innovative strategies
- Isotope drug studies in man
- Bioequivalence Criteria
- Risks in bioequivalence assessment
- Requirement to determine the active principle
- SUPAC: scale-up and for post-approval changes
- Relevance of bioequivalence in approving generic drug products
- Electronic regulatory submission and review
- Drug application regulatory compliance
- New drug quality assessment
- Targeted Therapeutics & Nanomedicine
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Advances In Bioavailability Conference Speakers
Recommended Sessions
- Advances In Bioavailability
- Analytical Method Development and Validation
- Bioavailability And Bioequivalence Studies
- Biopharmaceutics Classification System
- Clinical Studies
- Contract Research Organizations
- Drug Evolution Process of IND, NDA & ANDA
- Drug Formulation Procedures
- Drug Product Manufacturing
- Entrepreneur Investment
- Factors Affecting Bioavailability
- Formulation
- Medicinal Chemistry
- Novel Drug Delivery System
- Nutrient Bioavailability
- Preformulation Studies
- Regulatory Requirements
- Role of API In Research & Development
- Shelf Life & Stability Studies
- Traditional Medicine
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- Pharmacogenomics and Precision Medicine - Pharmacology-2025 (Spain)
- Pharmacogenomics in Cardiovascular Medicine - Cardiovascular-2025 (France)
- Pharmacokinetics and Drug Metabolism Modeling - Drug Delivery-2025 (France)
- Pharmacokinetics and Drug Optimization Strategies - Euro Antibiotics 2025 (Netherlands)
- Pharmacokinetics and Pharmacodynamics - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Pharmacokinetics and Pharmacodynamics - Pharmacology-2025 (Spain)
- Pharmacokinetics and Pharmacodynamics - Euro Pharmacology 2025 (France)
- Pharmacokinetics and Pharmacodynamics - Drug Delivery-2025 (Netherlands)
- Pharmacokinetics and Pharmacodynamics in Cardiology - Cardiovascular-2025 (France)
- Pharmacokinetics and Pharmacodynamics in Drugs - PHARMACEUTICA 2025 (Germany)
- Pharmacological Approaches to Myocardial Ischemia - Cardiovascular-2025 (France)
- Pharmacological Interventions in Mental Health - Euro Pharmacology 2025 (France)
- Pharmacological Management of Cardiovascular Risk Factors - Cardiovascular-2025 (France)
- Pharmacology and Toxicology - MedTech-2025 (Switzerland)
- Pharmacology in Public Health - Pharmacology-2025 (Spain)
- Pharmacovigilance & Drug Safety - Pharma Expo-2026 (Thailand)
- Pharmacovigilance & Post-Marketing Safety - Biologics Meet 2026 (UK)
- Pharmacovigilance and Drug Safety - Pharmacology-2025 (Spain)
- Pharmacovigilance and drug safety - Pharmaceuticals-2025 (France)
- Pharmacy Practice - Pharmaceuticals-2025 (France)
- Phytochemistry - Naturalproducts 2025 (Germany)
- Population Health - Personalizedmedicine-2025 (Switzerland)
- Post-Marketing Surveillance Insights - Clinical Trials Congress-2025 (France)
- Post-Trial Closed Communities - Clinical Trials Congress-2025 (France)
- Precision Medicine - Personalizedmedicine-2025 (Switzerland)
- QC & QA: Quality control and Quality assurance - MedTech-2025 (Switzerland)
- Quality by design (QbD) approach - MedTech-2025 (Switzerland)
- Quantum Chemistry and Molecular Simulations - Euro MedChem and CADD 2025 (France)
- Radiopharmaceuticals - Pharmaceuticals-2025 (France)
- Rapid Diagnostic Tools in Clinical Microbiology - Euro Antibiotics 2025 (Netherlands)
- Rare Cancers: Spotlight on Precision Oncology - ORPHAN DRUGS 2025 (France)
- Rare Disease Startups: Innovation and Investment Insights - ORPHAN DRUGS 2025 (France)
- Rare Neurological Disorders Take Center Stage - ORPHAN DRUGS 2025 (France)
- Regulatory Affairs & Global Approval - Biologics Meet 2026 (UK)
- Regulatory Affairs and Drug Approval - Pharmacology-2025 (Spain)
- Regulatory Affairs and Drug Safety - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Regulatory Affairs and Intellectual Property Rights - Future Pharma 2025 (Netherlands)
- Regulatory Affairs and Quality Assurance - Drug Delivery-2025 (Netherlands)
- Regulatory Authority Compliance - MedTech-2025 (Switzerland)
- Regulatory Harmonization & Compliance - Biologics Meet 2026 (UK)
- Regulatory Science and Clinical Trial Innovations - Euro Antibiotics 2025 (Netherlands)
- Regulatory Science and Translational Medicine - Drug Delivery-2025 (France)
- Role of Gut Microbiome in Cardiovascular Health - Cardiovascular-2025 (France)
- Role of Inflammation in Cardiovascular Diseases - Cardiovascular-2025 (France)
- Semi-Solid Dosage Forms - Formulations 2025 (France)
- Sexually Transmitted Bacterial Infections and Resistance Trends - Euro Antibiotics 2025 (Netherlands)
- Single-Use Technologies in Production - Biologics Meet 2026 (UK)
- Smart Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Smart Drug Delivery Systems - Formulations 2025 (France)
- Smart Polymers and Biomaterials - Drug Delivery-2025 (Netherlands)
- Smart Polymers and Responsive Drug Carriers - Drug Delivery-2025 (France)
- Solid Dosage Forms - Formulations 2025 (France)
- 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 Drug Delivery and Precision Medicine - Drug Delivery-2025 (France)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Targeted Therapies in Cardiovascular Regeneration - Cardiovascular-2025 (France)
- Targeting the Renin-Angiotensin-Aldosterone System (RAAS) - Cardiovascular-2025 (France)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Spain)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Transdermal and Intradermal Delivery Systems - Drug Delivery-2025 (Netherlands)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Trending: Digital Health and Telemedicine for Rare Care - ORPHAN DRUGS 2025 (France)
- Types of Formulations - Formulations 2025 (France)
- Vaccine Delivery Technologies - Drug Delivery-2025 (Netherlands)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Veterinary Pharmacology - Pharmacology-2025 (Spain)
- Women in Rare Disease Leadership and Science - ORPHAN DRUGS 2025 (France)