Bioavailability Studies and Assessment
Bioavailability is a subcategory of pharmacological absorption. Bioavailability is generally assessed by finding the area under the plasma concentration–time curve. The factors affecting bioavailability are Pharmaceutics factors, physicochemical properties of drug, Dosage form characteristics & Pharmaceutic Ingredients, Patient related factors like age, Routes of administration (Parenteral, Rectal, Oral, and Topical) etc.
Conducting a BA study enables assessment of the impact of route of administration on BA and defines the absolute BA of the drug released from the drug product. BA for a given formulation provides an assessment of the relative fraction of the orally administered dose that is absorbed into the systemic circulation. If the reference standard is an IV dose, it is referred as Absolute Bioavailability. If the reference standard is any other dosage form than IV it is referred as Relative Bioavailability
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Bioavailability Studies and Assessment Conference Speakers
Recommended Sessions
- Advances in Chromatography and Mass Spectrometry
- Analytical Method Development and Validation
- Bioavailability Studies and Assessment
- Bioavailability Studies and Assessment
- Bioavailability Studies and Assessment
- Bioavailability Studies and Assessment
- Bioavailability Studies and Assessment
- Bioequivalence Studies and Assessment
- Bioequivalence Studies and Assessment
- Clinical Research Vs Clinical Trails
- Clinical Research Vs Clinical Trails
- Contract Research Organizations
- Formulation R&D
- Industrial Pharmacy& Physical Pharmacy
- Latest Drug Development instruments
- Nano Medicine & Nano Technology
- NMR and Analysis of Small Organic Molecules
- Novel Approaches to Analytical and Bio analytical Methods
- Pharma Regulatory affairs
- Pharmaceutical Formulations
- Pharmaceutical Freeze Drying Technology
- Recent advancements in BA/BE Research
- Recent approaches to Biosimilars
- Role of Chemistry in Pharmaceuticals
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