[학술]
[DIA] Unpacking the ICH E6 (R3) GCP Guideline for Sponsors – Join Our Free Webinar (Aug 27, 2025)
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약학대학교학팀
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오정은
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작성일
2025-08-20
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조회수
75
Unpacking the ICH E6 (R3) Good Clinical Practice (GCP) Guideline for Sponsors |
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Wednesday, August 27, 2025 3:00–5:00PM SGT / 4:00–6:00PM KST
Participation Fee: Free |
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This upcoming webinar is designed to provide practical insights into the sponsor responsibilities for interventional clinical trials, as outlined in the ICH E6 (R3) Good Clinical Practice (GCP) guideline. Featuring members of the ICH E6 (R3) Expert Working Group from both regulatory authorities and industry, the session will explore key principles, sponsor oversight, and data governance strategies aligned with evolving regulatory frameworks. Whether you are a sponsor, CRO, regulatory professional, or clinical trial stakeholder, this session will offer valuable guidance on applying GCP principles effectively in today’s clinical research environment. |
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Featured Topics and Speakers |
| - 3:00-3:05 Introduction
- Jing Ping Yeo (Precision for Medicine) - 3:05-3:25 Principles of ICH E6 (R3) Good Clinical Practice (GCP)
- Sumitra Sachidanandan (HSA, Singapore) - 3:25-4:00 Sponsor Oversight of Clinical Trials
- Gabriele Schwarz (BfArM, Germany) - 4:00-4:35 Data Governance
- Rebecca Stanbrook (Novartis Pharma AG) - 4:35-4:50 Q&A
- All speakers - 4:50-5:00 Closing Remarks
- Young Joo Park (DIA Korea, Singapore and SEA)
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