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HUM-MOLGEN
-> Events
-> Meetings and Conferences |
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February 17, 2022 |
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xtalks.com, webinar
Thursday, March 17, 2022 | 11:00am JST (Japan) / 7:30am IST (India) / 10:00am CST (China) / 11:00am
Who Should Attend?This program is intended for pharmaceutical and biotech professionals involved in: - Outsourcing Procurement
- Project Management
- Medical Affairs
- Regulatory Affairs
- Clinical Development
What You Will LearnWebinar attendees will learn: - The impact of recent regulatory reforms, including the Human Genetic Resources Administration of China (HGRAC) regulation
- Best practices for operational oversight and governance
- Practical tips and solutions for developing an effective communications plan
- How to address escalations
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Organized by:
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xtalks.com |
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Invited Speakers:
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Speaker
Qing Liu, MPH, MBA, Director, Project Management, ICONQing has been with ICON since August of 2016 and now is the head of ICON China project management team. Qing holds two master’s degrees of MPH from Peking University and MBA from Asia Metropolitan University. She has 15 years clinical research experience including global phase I/II/III/IV clinical trials experience and has dedicated generic and oncology drug development experience (APAC and US). Qing worked in pharma (Novartis, Sihuan Pharma group) and CROs (PPD, Incrom) prior to joining ICON. |
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Deadline for Abstracts:
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Registration:
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https://xtalks.com/webinars/a-guide-to-conducting-clinical-trials-in-china/
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E-mail:
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shunte@xtalks.com
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