Global Summit on Generic Drugs and Quality Control

Key Topics

• Modernization of Bioequivalence Standards for Generic Products
• Best Practices & Strategies for Generic Drug Development
• Bioequivalence approaches for complex injectable API and formulations
• Application of Quantitative systems pharmacology (QSP)
• Pharmaceutical Quality Assurance
• Generic Animal Drug
• Acceptance of Generic Drugs by People
• Challenges of Manufacturing Generic Drugs
• Biosimilars
• Challenges of Marketing Generic Drugs
• Quality by Design (QbD) for generic drugs
• Current Good manufacturing practices (CGMP)
• Super Generic drugs and Bio Betters
• Global Generic Trends
• Complex Generic Drug Product
• Patent Access& Intellectual property& FDA Regulations
• Generic Drug Market

Who should Attend

• Research & Development
• Clinical Researchers
• Public Health Advisors
• Pharmacists
• Pharmacology
• Regulatory Affairs
• Quality Assurance/Control
• Safety/Pharmacovigilance
• CMC/ GMP
• Manufacturing companies
• Veterinarians
• Medical practitioners
• Students