Bioavailability And Bioequivalence Studies
Amount of a substance that becomes available reaches the target organ or systemic circulation to an organism's body for bio-activity when introduced through ingestion, inhalation, injection, or skin contact. Rate of bioavailability depends on factors such as the type of the substance and the composition of diet.
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.
- Factors influencing bioavailability
- Methods for in vitro dissolution and bioavailability assays
- Liquisolid technology
- Prodrugs
- Oral drugs
- Therapeutic systems
- Food effect
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Bioavailability And Bioequivalence Studies 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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- Recent Advancements in Medicinal Pharma - PHARMA MEDICINAL CHEMISTRY 2025 (Canada)
- Recent Advances in Pharmacology and Toxicology - Pharmacology 2025 (France)
- Recent Advances in Pharmacology and Toxicology - Pharmacology 2025 (France)
- Regenerative Medicine - Pain Management 2025 (Switzerland)
- Regulatory Affairs and Drug Safety - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
- Regulatory Affairs and Intellectual Property Rights - Future Pharma 2025 (Netherlands)
- Regulatory Affairs and Quality Assurance in Pharmaceutics - Pharmaceutica-2025 (Canada)
- Regulatory Authority Compliance - MedTech-2025 (Switzerland)
- Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2025 (France)
- Regulatory Updates on Biosimilars - Eurobiosimilars 2025 (France)
- Role of Gut Microbiome in Cardiovascular Health - Cardiovascular-2025 (France)
- Role of Inflammation in Cardiovascular Diseases - Cardiovascular-2025 (France)
- Safety Pharmacology - Pharmacology 2025 (France)
- Smart Drug Delivery Systems - Pharmatech 2025 (Canada)
- Smart Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Smart Polymers for Drug Delivery - Pharmaceutica-2025 (Canada)
- Sustainability and Global Health Biotechnology - Biotech-2025 (France)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
- Targeted Drug Delivery and Controlled Release Systems - PHARMA CONFERENCE-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)
- Toxicology - Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
- Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
- Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (France)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (France)