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SUMMARY:2025 PDA/FDA Joint Regulatory Conference
DESCRIPTION:Returning to Washington\, DC for the 34th year\, PDA’s annual September regulatory conference builds on over three decades of success as the industry’s trusted resource to inform\, educate\, and guide professionals and organizations. \nThe PDA Regulatory Conference 2025 continues the tradition of delivering impactful content that supports the development and implementation of effective quality systems across the product lifecycle. Sessions will focus on strategies to manage manufacturing and quality risks while driving operational excellence and sustainable compliance. \nThe Conference will emphasize the vital role of robust quality systems\, facility and process design\, supplier and raw material oversight\, industrial modernization\, quality risk management\, and strong partner relationships as fundamental to maintaining Current Good Manufacturing Practice (CGMP) compliance. \nCase studies presented throughout the Conference will offer real-world examples of how sustainable compliance can drive consistent product quality and reliable supply. \nIn addition to the Regulatory Conference\, PDA is offering a variety of workshops and training courses on Thursday and Friday (11-12 Sep) – giving attendees the opportunity to deepen their learning through practical\, hands-on application. \n\nPDA/PQRI Advancing Artificial Intelligence in the Pharmaceutical Industry Workshop 2025\nAseptic Processing Essentials Workshop\nCMC Regulatory Compliance Strategy for Biopharmaceutical Manufacturing Training Course\nContamination Control Strategy Essentials Workshop\nDecision-Making in Pharma Manufacturing: Ethics\, Compliance\, and Resilience Training Course\nFundamentals of Quality Risk Management Training Course\nGxP Auditing Logistics and Inspection Readiness Training Course (Including Mock Activity)\nMeasuring Quality Culture using PDA’s Assessment Tool Training Course\nQuality and Compliance Management for Virtual Companies Training Course\n\nThe PDA Regulatory Conference 2025 remains your trusted source for CGMP insights. Registration is now open with early pricing!
URL:https://sterile.com/event/2025-pda-fda-joint-regulatory-conference/
LOCATION:Westin Washington\, DC Downtown\, 999 9th Street\, NW\, Washington\, DC\, 20001\, United States
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SUMMARY:2024 PDA/FDA Joint Regulatory Conference
DESCRIPTION:FDA and Parenteral Drug Association (PDA) will host the 33rd Joint Regulatory Conference to emphasize the role of effective quality systems in ensuring an ongoing state of control throughout the product lifecycle. \nThe conference will: \n\nfocus on the vital role of robust quality systems\, facilities\, processes\, raw material quality\, supplier relationships\, industrial modernization and quality risk management\, which are fundamental to current good manufacturing practice (CGMP) compliance\ninclude case studies to provide practical insights and illustrate how sustainable compliance establishes the foundation for quality and supply consistency\nhighlight international collaboration efforts that improve quality and benefit consumers
URL:https://sterile.com/event/2024-pda-fda-joint-regulatory-conference/
LOCATION:Westin Washington\, DC Downtown\, 999 9th Street\, NW\, Washington\, DC\, 20001\, United States
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