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Event Title
2026 PDA/FDA Joint Regulatory Conference
September 14 - 16, 2026


Date:
September 14 - 16, 2026
Day1:
Mon, Sep 14 7:00 a.m. - 06:00 p.m. ET
Day2:
Tue, Sep 15 7:00 a.m. - 06:00 p.m. ET
Day3:
Wed, Sep 16 7:00 a.m. - 03:30 p.m. ET

About

FDA and Parenteral Drug Association (PDA) will host the 2026 PDA/FDA Joint Regulatory Conference, Excellence in CGMP: Ensuring Quality, Protecting Patients, in Washington, D.C.

The conference will offer practical insights on current good manufacturing practice (CGMP) compliance, quality systems, risk-based manufacturing, supply chain oversight and industrial modernization through expert-led discussions and real-world case studies.

The conference will explore regulatory priorities, emerging technologies and quality challenges through expert-led discussions, case studies and direct engagement with regulators and industry leaders.

Topics will include:

  • FDA Center and Office Updates
  • AI in Regulatory Oversight and Inspection Readiness
  • Inspection Readiness and Pre-Approval Inspections
  • Corrective and Preventive Action (CAPA) and Effectiveness Checks
  • Data Governance and Quality Risk Management
  • Change Management and Quality Systems
  • Workforce Development and CGMP Training
  • Global Regulatory Collaboration

Visit the PDA/FDA Joint Regulatory Conference 2026 webpage for additional information.

Who should attend:

  • Quality assurance and quality systems professionals
  • Regulatory affairs and compliance leaders
  • CGMP manufacturing and technical operations professionals
  • Validation, auditing and inspection readiness professionals
  • Data governance and digital quality leaders
  • Supplier quality and external partner professionals
  • FDA and global health authority representatives
  • Cross-functional quality and compliance professionals
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