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Jamis, Lina
Synthego Corporation
What are the Requirements for an IND Submission?
Location/Room:510B
Lina Jamis
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Jeary, Theresa
BSI Group
Drug-Device Combination Products: The Why Behind the Regulatory Strategy
Location/Room:510B
Theresa Jeary
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Jeiter, Tonia
TÜV SÜD Product Service GmbH
Latest Updates on Clinical Evidence – Panel Discussion with a Consultant and 3 Notified Bodies
Location/Room:511F
Tonia Jeiter
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Jennings, Jocelyn
Mycovia Pharmaceuticals, Inc.
RAPS Store Stage: Meet the Authors - Regulation of Regenerative Medicines: A Global Perspective
Location/Room:RAPS Store Stage (Level 2 Registration Foyer)
Jocelyn Jennings
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Jew, Korinne
Medtronic
Transforming Patient Engagement in Medical Technologies' Evolving Regulatory Landscape
Location/Room:510B
Korinne Jew
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Joneckis, Christopher
US FDA
Health Authority Forum: CBER & CDER - FDA’s Center for Biologics Evaluation and Research (CBER) & Center for Drug Evaluation and Research (CDER)
Location/Room:510B
Christopher Joneckis
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Jump, Michelle
MEDSEC
Medical Device Cybersecurity: Planning a Global Strategy
Location/Room:513B
Michelle Jump
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Jung, Yoon Sik
University of Southern California
Student Capstone Poster Display: Survey of Clinical Trial Data of Immune Checkpoint Inhibitors – Avelumab and Cemiplimab
Location/Room:Exhibit Hall: Career Central (Booth 633)
Yoon Sik Jung
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Student Capstone Poster Display: Survey of Clinical Trial Data of Immune Checkpoint Inhibitors – Avelumab and Cemiplimab
Location/Room:Exhibit Hall: Career Central (Booth 633)
Yoon Sik Jung
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