Your life sciences partner across the entire product lifecycle

QbD Group is the European Expert specialized in quality assurance, regulatory compliance, clinical services and digital solutions for the Medical Device, IVD, Pharma and Biotech industry.

QbD Group is a service partner for companies worldwide to ensure they meet the highest quality and safety standards, from idea to patient.

Discover our services

Full life cycle support

From idea to patient, we guide you through every stage as a full-service partner - supporting 1,200+ start-ups, scale-ups, and global leaders in Life Sciences to maximize asset value.

Trusted expertise at scale

With 600+ in-house professionals and deep specialization in pharma, MedTech, and IVD, we solve complex challenges across quality, regulatory, clinical, and digital domains.

Tailored, cost-effective solutions

We design fit-for-purpose, right-sourced solutions with lean project setups and solid project management - delivering quality results efficiently and effectively.

Deliver on our promise

We get things done. Our hands-on teams take ownership, solve problems proactively, and deliver on time with high-quality standards and unwavering commitment.

Agile collaboration that works

We embed into your team with flexibility and transparency, working with joy to drive shared success and build long-term partnerships.

Your gateway to the European market

We help global Pharma and MedTech companies enter and thrive in Europe through strong GxP know-how, regulatory strategy, clinical evidence, importation, and life cycle expertise.

Industries we cover

We specialize in supporting life sciences companies across various key industries.

With expertise in each sector, we help navigate complex challenges to bring innovative products to market efficiently and compliantly. Discover more about our core industries here.

Pharma & Biotech

Medical Devices

In Vitro Diagnostics

Our services

QbD Group offers a comprehensive suite of services that cover critical areas in life sciences product development, launch and commercialization.

Explore our 8 specialized services designed to ensure success at every stage.

Regulatory Affairs

Quality Assurance

Lab Services

Qualification & Validation

Vigilance

Clinical

Software Solutions & Services

Toxicology

Accelerate your entry into the European market

From regulatory strategy and GMP compliance to batch release and market authorization, QbD Group offers the full support you need.

Rely on our end-to-end expertise to make your entry into the European market smooth, compliant, and efficient.

Latest news

QbD Group welcomes Diane Fairweather as Division Head Clinical

27 May 2025

QbD Group welcomes Dr. Diane Fairweather as Division Head...

23 May 2025

QbD Group awarded Gold Label as Best Managed Company 2025

6 May 2025

Dr. Angeles Escarti-Nebot joins QbD Group as Division Head...

10 Feb 2025

Azierta fully integrated into QbD Group

Discover our expert content

Webinar

Pharmacovigilance and Risk Management in Innovative Therapies: A Challenge in Drug Safety

Explore pharmacovigilance in cell, CAR T, and RNA therapies. Join our webinar to tackle tomorrow’s drug safety and risk management challenges.

Webinar

Extractables & Leachables in Pharma: Navigating Evolving Regulations and Toxicological Challenges

This webinar aims to provide a comprehensive overview of Extractables and Leachables (E&L) in pharmaceutical products, highlighting regulatory complexities, toxicological challenges, and practical approaches to study design and risk assessment across the product lifecycle.

Whitepaper

Digital Health - Exploring the landscape and future opportunities

This whitepaper informs you about digital health, key technology pillars, and new opportunities to anticipate future trends in your healthcare sector.