Live Training | Key Messages for Conducting a Clinical Study in the EU

Written by Amé Huige | Feb 11, 2026 8:24:32 AM

Date: 9 March 2026 (additional 1-on-1 meetings with our experts on 10 March)

Location: 3^rd Floor YunGuan Hall (三楼云冠厅) of Shanghai Hongqiao Airport Boyue Hotel – AirChina (上海中航泊悦酒店), Shanghai, China

Time: 14:00 - 18:00 CST

Price: 1000 CNY

Language: English

Introduction

Conducting a clinical study in the European Union requires a solid understanding of regulatory expectations, Good Clinical Practice, and country-specific requirements. With increasing scrutiny from competent authorities and ethics committees, getting it right from the start is critical.

On 9 March 2026, Qserve invites you to a live, in-person training in Shanghai focused on the key messages for successfully conducting clinical studies in the EU. This interactive afternoon session will guide you through ISO 14155, EU regulatory frameworks, safety and SAE reporting, and common pitfalls seen in clinical investigations.

Led by experienced trainers and supported by local expertise, this training not only builds regulatory knowledge but also introduces Qserve and Qserve CRO as your trusted partners for clinical research, regulatory strategy, and professional training. Whether you are preparing your first EU clinical study or looking to strengthen existing processes, this session delivers practical insights you can apply immediately.

Agenda

13:30 - 14:00 CST | Registration and welcome
14:00 - 14:15 CST | Qserve Introduction, Company Overview, and CRO Services
14:15 – 15:15 CST I General standards ISO 14155, Good Clinical Practice

Scope and objectives of ISO 14155
Key principles and responsibilities
Practical implications for clinical investigations

15:15 - 15:30 CST | Coffee and Tea Break
15:30 - 16:30 CST | Country specifics for the EU

Regulatory framework in the EU
National competent authorities and ethics committees
Key differences between EU member states
Practical examples and common pitfalls

16:30 - 16:45 CST | Coffee and Tea Break
16:45 - 17:45 CST | Safety and SAE

Safety reporting requirements
Definitions and classification of adverse events and SAE
Reporting timelines and responsibilities
Case studies and best practices

17:45 - 18:00 CST | Wrap-Up and Q&A.

Secure your seat for this exclusive live training in Shanghai. Places are limited.

Register now to gain hands-on EU clinical investigation insights and connect with Qserve’s clinical and regulatory experts. We look forward to welcoming you in Shanghai!

We are offering 1-on-1 meetings with our experts on March 10. If you are interested, please email info.china@qservegroup.com to discuss and book your slot.

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