Bioavailability and bioequivalence studies are critical in evaluating the effectiveness and safety of pharmaceutical products. Bioavailability refers to the extent and rate at which the active ingredient of a drug reaches the systemic circulation, ensuring that the drug is available to exert its therapeutic effects. These studies are essential for understanding how various factors, such as formulation, route of administration, and metabolic variations, influence drug absorption and overall efficacy. Bioequivalence studies, on the other hand, compare the bioavailability of a generic drug to its branded counterpart, ensuring that both produce similar therapeutic effects when administered in equivalent doses. These studies help confirm that generic medications are as safe and effective as their branded versions, promoting greater access to affordable treatments. Through rigorous bioavailability and bioequivalence testing, pharmaceutical companies ensure the reliability and consistency of drugs, enhancing patient care and confidence in treatment options.
Consolato M Sergi
Universities of Alberta and Ottawa, Canada
Vladlen Slepak
University of Miami Miller School of Medicine, United States
Andreas M Papas
Antares Health Products, United States
Sergey Suchkov
The Russian University of Medicine and Russian Academy of Natural Science-Moscow, Russian FederationSubmit your abstract Today
Title : Medical liver biopsy: Toward a personalized approach
Consolato M Sergi, Universities of Alberta and Ottawa, Canada
Title : Ectopically expressed olfactory receptors as an untapped family of drug targets and discovery of agonists and antagonists of OR51E1, an understudied G Protein-Coupled Receptor
Vladlen Slepak, University of Miami Miller School of Medicine, United States
Title : Mathematical modeling the disc diffusion test: Antibacterial activity of copper-doped SnO2
Paulo Cesar De Morais, Catholic University of Brasilia, Brazil
Title : Emerging formulation and delivery applications of Vitamin E TPGS
Andreas M Papas, Antares Health Products, United States
Title : Personalized and Precision Medicine (PPM) as a unique healthcare model through design-inspired biotech- & biopharma-driven applications and upgraded business marketing to secure the human healthcare and biosafety
Sergey Suchkov, The Russian University of Medicine and Russian Academy of Natural Science-Moscow, Russian Federation
Title : Design and evaluation of exo-itc: A bilayer fibrous system for controlled exosome delivery in dermatological applications
Luis Jesus Villarreal Gomez, FCITEC - Universidad Autónoma de Baja California, Mexico
Title : Macitentan/Tadalafil Combination– An additional value in pharmacotherapy of pulmonary arterial hypertension
Miroslav Radenkovic, University of Belgrade, Serbia
Title : Understanding drug transport in plasma: The role of protein binding
Saad Tayyab, UCSI University, Malaysia
Title : Drug development - Importance, trends and digital transformation
Gurpreet Singh, IQVIA, United Kingdom
Title : Navigating the regulatory landscape for nanotechnology-based pharmaceuticals: challenges and strategies for harmonization
Srividya Narayanan, Northeastern University, United States