2nd International Conference on Bioequivalence & Bioavailability (ICBEBA-2019)

2nd International Conference on Biequivalence & Bioavailability (Bioequivalence & Bioavailability-2019),which will be held during August 19-20, 2019 in Barcelona, Spain, is now an established event, attracting global participant’s intent on sharing, exchanging and exploring new avenues of Bioequivalence & Bioavailability and related research and latest developments. The event will have 5-6 world level (Highly cited class) plenary speakers, established Keynote speakers, active Invited speakers and fresh contributed speakers. In addition, a variety of poster presentations along with workshops and special sessions would be interested in the audience.

Topics:

 - Drug Targeting and Drug Development
 - Drug Discovery, Development and Posology
 - Bioavailability and Bioequivalence studies
 - Clinical Research
 - Drug Toxicology and Interaction
 - Food and Nutritional Toxicology
 - Genetic and Molecular Toxicology
 - Immunopharmacology and Immunotoxicology
 - Neuro and Cardiovascular Pharmacology
 - Novel Drug Delivery System
 - Pharmaceutical Analysis
 - Pharmaceutical Formulations
 - Pharmacogenetics and Pharmacogenomics
 - Pharmacokinetics between Pediatric and Geriatrics
 - Pharmacology and Toxicology
 - Pharmacotherapeutics and Drug Toxicity
 - Pharmacovigilance
 - Psychopharmacology and Pharmacoepidemiology
 - Chromatography
 - Spectrometry
 - Nanomedicals
 - Analytical Biochemical Techniques
 - Bioanalysis and Microbiology
 - Clinical Cancer Trials
 - Regulatory Requirements Of Pharmaceutical Products
 - Bioequivalence Study Protocols
 - Challenges in Drug design
 - Clinical Research Vs Clinical Trails
 - Nutrient Bioavailability
 - Advances in Assessment of Bioequivalence
 - Surgery And Anesthesiology
 - Computational Biomedicines
 - Pharmacokinetics
 - Toxicology
 - Pharmaceutical and Biological Chemistry
 - Regulatory Requirements Of Pharmaceutical Products
 - Screening And Drug Design
 - Pharmaceutical Technology
 - Biopharmaceutics - Advances and Applications
 - Drug Safety and Drug Toxicity - Pharmacovigilance Scope
 - Public Health Nutrition
 - Bioavailability - Academic and Industry Overview
 - Formulation Studies for Clinical Research
 - Pharmacology - PK PD Approach
 - Drug Design and Development - Challenges and Approaches
 - BA-BE Perspectives for Drug Products
 - Analytical Biochemical Techniques
 - Bioequivalence Antipsychotics
 - Analytical Chromatography
 - Bioequivalence Study Protocols
 - Clinical Drug Trial
 - Drug Delivery Using Nanotechnology
 - HPTLC
 - Peptidomimetic
 - FDA Bioequivalence
 - Computational Biomedicine
 - Clinical Cancer Trials