BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Veltek Associates, Inc. - ECPv6.16.5//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Veltek Associates, Inc.
X-ORIGINAL-URL:https://sterile.com
X-WR-CALDESC:Events for Veltek Associates, Inc.
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20240310T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20241103T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20250309T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20251102T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20260308T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20261101T060000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250908T080000
DTEND;TZID=America/New_York:20250910T170000
DTSTAMP:20250609T141723Z
CREATED:20250609T141723Z
LAST-MODIFIED:20250609T141723Z
UID:70048-1757318400-1757523600@sterile.com
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
ATTACH;FMTTYPE=image/jpeg:https://sterile.com/wp-content/uploads/PDARegulatory2025-1200x630-1.jpg
END:VEVENT
END:VCALENDAR