---
title: "Newsletter | Life Sciences Insights | QbD Group"
description: "Subscribe to QbD Group's newsletter for expert regulatory insights, compliance guidance, and industry analysis delivered to your inbox."
url: https://qbdgroup.com/en/newsletter
type: "Page"
language: en
publisher: "QbD Group"
citation: "QbD Group, \"Newsletter | Life Sciences Insights | QbD Group\", https://qbdgroup.com/en/newsletter"
---

[About us](https://qbdgroup.com/en/about-qbd)

[Knowledge center](https://qbdgroup.com/en/knowledge-center)

[Events](https://qbdgroup.com/en/events)

[Careers](https://careers.qbdgroup.com)

NEWSLETTER

# Stay ahead in life sciences

Expert regulatory insights, compliance guidance, and industry analysis, delivered to your inbox every two weeks.

No spam, ever. Unsubscribe anytime. Read our [Privacy Policy](https://qbdgroup.com/en/privacy-policy).

NEWSLETTER

## What you'll receive

Curated content from our team of 250+ life sciences consultants across Europe.

### Regulatory intelligence

Be the first to know about regulatory shifts impacting pharma, biotech, and medical devices.

### Expert analysis

Deep-dive articles from seasoned consultants with decades of hands-on GxP experience.

### Compliance insights

Practical guidance on quality management, validation, and audit-readiness.

### Event & webinar alerts

Early access to webinars, workshops, and industry events.

PREVIEW

## See what lands in your inbox

A sneak peek at recent editions of the QbD Group newsletter.

QbD INSIGHTS

Edition #47 · Jan 2026

Bi-weekly

Featured

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

The latest guidance from the European Commission clarifies key requirements for legacy devices…

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

Bi-weekly

Featured

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

## Don't miss a beat

Join thousands of life sciences professionals who rely on our insights to stay compliant and competitive.

---

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