---
title: "Newsletter | 生命科学洞察 | QbD Group"
description: "订阅QbD Group通讯，获取专家法规洞察、合规指导和行业分析。"
url: https://qbdgroup.com/zh-cn/newsletter
type: "Page"
language: zh-cn
publisher: "QbD Group"
citation: "QbD Group, \"Newsletter | 生命科学洞察 | QbD Group\", https://qbdgroup.com/zh-cn/newsletter"
---

[关于我们](https://qbdgroup.com/zh-cn/about-qbd)

[知识中心](https://qbdgroup.com/zh-cn/knowledge-center)

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通讯

# 领先于 生命科学

专家法规洞察、合规指导和行业分析，每两周直达您的收件箱。

绝无垃圾邮件。随时退订。阅读我们的 [隐私政策](https://qbdgroup.com/en/privacy-policy).

通讯

## 您将收到什么

来自我们遍布欧洲的250+名生命科学顾问团队精选的内容。

### 法规情报

率先了解影响制药、生物技术和医疗器械的法规变化。

### 专家分析

来自经验丰富顾问的深度文章，拥有数十年GxP实践经验。

### 合规洞察

关于质量管理、验证和审计准备的实用指南。

### 活动与网络研讨会提醒

提前获取网络研讨会、工作坊和行业活动信息。

预览

## 看看您的收件箱会收到什么

QbD Group通讯近期版本预览。

QbD INSIGHTS

Edition #47 · Jan 2026

双周刊

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EU MDR Transition: What Manufacturers Need to Know Before the 2027 Deadline

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IVDR Update: Notified Body capacity report, current state and projections

Industry Trend: AI-driven pharmacovigilance, regulatory expectations in 2026

Upcoming: Free webinar on Post-Market Surveillance best practices, Feb 12

QbD INSIGHTS

Edition #46 · Dec 2025

双周刊

推荐

CDx & Companion Diagnostics: Navigating the Evolving EU Regulatory Landscape

As precision medicine advances, companion diagnostic regulation is catching up. Here's your roadmap…

White Paper: Quality by Design in pharmaceutical development, 2025 edition

Compliance Alert: EMA updates GMP Annex 1, key changes for sterile manufacturing

Case Study: How we helped a biotech startup achieve EU market launch in 9 months

## 不错过任何动态

加入数千名依赖我们洞察保持合规和竞争力的生命科学专业人士。

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Source: https://qbdgroup.com/zh-cn/newsletter — © QbD Group. Quote freely with attribution and a link back.