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X-WR-CALDESC:Events for CITI Program
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DTSTART;VALUE=DATE:20251007
DTEND;VALUE=DATE:20251010
DTSTAMP:20260405T181802
CREATED:20250912T145303Z
LAST-MODIFIED:20250912T145303Z
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SUMMARY:CITI Program to Exhibit at RAPS Convergence 2025
DESCRIPTION:Visit CITI Program at Exhibit Booth #910\nCITI Program will join The Regulatory Affairs Professionals Society (RAPS) at their 2025 Convergence from October 7-9\, 2025. RAPS is the world’s leading organization dedicated to professionals in regulatory and quality roles across the healthcare product landscape\, including medical devices\, pharmaceuticals\, biologics\, diagnostics\, and digital health. \nSession tracks include: \n\nDevices (including Medical Devices and In Vitro Diagnostics)\nPharmaceuticals (including Biologics and Drugs)\nBroad Interest (Cannabidiol\, Health-Related Foods\, AI\, Cybersecurity\, Data Transparency\, Inspections & Audits)\nSkill Building\n\nVisit the conference page for more information.
URL:https://about.citiprogram.org/event/citi-program-to-exhibit-at-raps-convergence-2025/
LOCATION:David L. Lawrence Convention Center\, 1000 Ft. Duquesne Blvd.\, Pittsburgh\, PA\, 15222\, United States
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DTSTART;TZID=America/New_York:20251007T090000
DTEND;TZID=America/New_York:20251008T150000
DTSTAMP:20260405T181802
CREATED:20250926T162030Z
LAST-MODIFIED:20251015T175233Z
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SUMMARY:Advancing Generic Drug Development: Translating Science to Approval 2025
DESCRIPTION:Join FDA experts at the 2025 Advancing Generic Drug Development Workshop\, an in-depth event exploring the transformative impact of the Generic Drug User Fee Amendments (GDUFA) Science and Research Program on generic drug development\, regulation\, and approval. \nThis workshop will cover key scientific and regulatory challenges in abbreviated new drug applications (ANDAs)\, provide insights into GDUFA III progress\, and spotlight innovative research in complex generics. \nKey Topics Include: \n\nResearch and methodologies to support guidance development on complex generic products including implant\, inhalation\, and topical products\nInnovative methodologies and design recommendations for demonstrating therapeutic equivalence\nCommon regulatory challenges and solutions for generic products with complex drug substances\, excipients\, and formulations\nKnown issues and practical strategies for addressing nitrosamine contamination in pharmaceutical products\n\nLearning Objectives: \n\nStay up-to-date with the latest advancements in science\, research\, guidance development\, and regulatory evaluation related to generic drug products\nRecognize and explain how the FDA’s GDUFA-funded research can be leveraged to support and inform generic drug development\nUtilize various strategies and methodologies to facilitate efficient generic drug development\n\nVisit the event page for more information.
URL:https://about.citiprogram.org/event/advancing-generic-drug-development-translating-science-to-approval-2025/
LOCATION:Online
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DTSTART;TZID=America/New_York:20251007T120000
DTEND;TZID=America/New_York:20251007T123000
DTSTAMP:20260405T181802
CREATED:20250925T162007Z
LAST-MODIFIED:20251015T175246Z
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SUMMARY:FAES Virtual Information Session: Hood College Partnership
DESCRIPTION:The Foundation for Advanced Education in the Sciences (FAES) is committed to advancing education and research in the biomedical sciences while supporting the educational needs of the NIH community. On October 7 at 12 PM\, FAES will host a virtual information session exclusively for the NIH community\, featuring Dr. April Boulton\, Associate Provost and Dean of the Graduate School at Hood College. This session will highlight flexible graduate degree and certificate options at Hood College and explain how FAES coursework may be applied toward those programs. \nVisit the event page for more information.
URL:https://about.citiprogram.org/event/faes-virtual-information-session-hood-college-partnership/
LOCATION:Online
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BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251007T140000
DTEND;TZID=America/New_York:20251007T150000
DTSTAMP:20260405T181802
CREATED:20250923T140110Z
LAST-MODIFIED:20260204T190105Z
UID:59137-1759845600-1759849200@about.citiprogram.org
SUMMARY:Free Live Webinar - The DOJ Bulk Data Transfer Rule
DESCRIPTION:The DOJ Bulk Data Transfer Rule\nTuesday\, October 7\, 2025 at 2:00 p.m. ET\nThis webinar introduces the Department of Justice’s new Bulk Data Transfer Rule (also called the Data Security Program Rule)\, which regulates transfers of sensitive health\, genomic\, and personal data to certain foreign countries. We will first examine why the rule was issued\, focusing on its national security and policy foundations\, and then outline its key requirements\, covered data\, and institutional implications. Determining applicability and organizational responsibilities requires a careful inventory of data. Attendees will gain both a primer on the rule itself and perspective on how it signals broader regulatory shifts in data governance\, research\, and compliance. \nRegister for additional free live webinars and available webinar replays. \n\n    \n        \n\n\n                            \n                    \n                        \n                        \n                        \n                           This Webinar Has Closed\n                        \n                        \n                    \n                                        Click below to browse our other upcoming webinars. \n                        \n\n\n\n                            \n                                Webinars Catalog
URL:https://about.citiprogram.org/event/free-live-webinar-the-doj-bulk-data-transfer-rule/
LOCATION:Online
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