Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans 2018

  • 08-09 Feb 2018
  • Washington, DC, United States

Description

Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans 2018 covers topics such as:

  • Basic and required pharmacokinetic principles including terminologies such as plasma drug concentration-time profiles/curves, rates of absorption and elimination, Cmax, Tmax, half-life, AUC, apparent volume of distribution, bioavailability/bioequivalence, etc
  • Dissolution and related physiological terms: Drug absorption, permeation, relevant GI tract environment
  • Defining quality of drugs/medicines and drug/medicinal products
  • Defining, and differentiating, drugs/medicines and drug/medicinal products
  • What is drug dissolution Testing and Why to conduct such tests?
  • Generic vs innovator`s products (Similarities and differences)
  • Drug Dissolution Testing vs Solubility determination
  • Dissolution theory, sink conditions and intrinsic dissolution rate
  • Dissolution Testing Apparatus
  • Drug Dissolution vs Drug Release Testing - Is there a difference?
  • Dissolution equipment qualification (Performance Tablets vs Mechanical Calibration)
  • Setting up a dissolution tester (e.g. Basket and paddle)
  • Dissolution Method Developments
  • Tolerances and results Interpretation
  • Linking Dissolution Results to Plasma Drug Levels

Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans 2018 brings together attendees with responsibilities in:

  • Setting up analytical methods (pharmacopeial, regulatory or in-house developed)
  • Pharmaceutical Development
  • Project Management
  • R & D, both analytical and formulation
  • Quality Assurance
  • Quality Control
  • Regulatory Affairs

Past Events

Important

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Event Categories

Business: Innovations, Quality assurance
Health & Medicine: Hematology, Medical device, Medical laboratories, Medical technology, Pharma
Science: Life Sciences & Biology

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