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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. 

Why do clients choose QbD Group?

Key differentiators shaped by our core JPEG values

Full life cycle support

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

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.

Your gateway to the European market​

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.

Tailored, cost-effective solutions

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

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​

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.

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.

Industries_Rendering_Pharma & Biotech

Pharma & Biotech

Industries_Rendering_Medical Devices

Medical Devices

Industries_Rendering_IVD

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.

regelatory_affairs

Regulatory Affairs

quality_assurance

Quality Assurance

lab_services

Lab Services

qualification_and_validation

Qualification & Validation

vigilance

Vigilance

clinical

Clinical

software_solutions_and_services

Software Solutions & Services

Tox blue

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.
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Latest news

QbD Group welcomes Diane Fairweather as Division Head Clinical
27 May 2025

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

QbD Group awarded Gold Label as Best Managed Company 2025
23 May 2025

QbD Group awarded Gold Label as Best Managed Company 2025

Dr. Angeles Escarti-Nebot joins QbD Group as Division Head Regulatory Affairs - QbD Group
6 May 2025

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

News - Azierta fully integrated into QbD Group - QbD Group
10 Feb 2025

Azierta fully integrated into QbD Group

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Discover our expert content

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Whitepaper

Audit Trail Review in GxP Environments

Learn how to implement a risk-based Audit Trail review strategy to enhance software compliance in GxP environments.
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Whitepaper

The Essential CSV & Digitalization FAQ for Life Sciences Companies

Get clear answers to real CSV questions from clients & experts. Download our FAQ and stay compliant, audit-ready, and confident in your Software Validation Strategy.
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Whitepaper

Digitalization in the Pharmaceutical Industry: And How to Stay Compliant

Digitalization and Pharma 4.0 drive digital transformation. Explore the role of CSV in pharma's digital journey.
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Case study

Validating a Complex Autoclave Load to Enhance Sterilization Efficiency

Discover how QbD Group helped a pharmaceutical facility in Barcelona optimize and validate a complex autoclave load, improving sterilization efficiency and manufacturing flexibility.