Pharmaceutical Lab Services

Quality by control

With over 25 years of experience, QbD Group's Lab Services provides high-quality analytical solutions tailored to the pharmaceutical industry. Our GMP-compliant laboratory combines efficient turnaround times, competitive pricing, and a flexible, personalized approach. Whether managing large volumes or complex projects, we deliver reliable results to meet your analytical needs with precision and expertise.

Efficient turnaround times

Our streamlined workflows and expert team deliver rapid, accurate results without compromising quality.

Competitive pricing

By optimizing processes and implementing lean workflows, we ensure high-quality services at prices that suit your budget.

Experience & personalized approach

With over 25 years of expertise, we support both multinational pharmaceutical companies and start-ups, tailoring solutions to your unique needs.

Uncompromising quality

Our highly skilled team conducts analyses using state-of-the-art equipment, operating under GMP conditions to ensure compliance and precision.

Industry context

Market Trends & Challenges

The demand for precision, speed, and compliance in lab services has never been greater. As industries face heightened regulatory scrutiny, the need for accurate testing and streamlined processes is paramount. From detecting impurities to ensuring batch stability, lab testing now demands advanced technology and skilled expertise.

Globalization adds complexity, with companies navigating varied regulations across regions. The push toward sustainability also creates new challenges, as industries look for innovative ways to validate environmentally friendly materials and processes.

QbD Group's Lab Services provide the expertise and tailored solutions needed to meet these demands. Whether it's method validation, stability testing, or batch release, we help businesses stay ahead by delivering reliable, actionable results.

Offerings

What we offer11

Cleaning Validation

Effective cleaning is essential to protect patient safety, and we can help you define a best practice approach in setting up plans and protocols for cleaning validation.

Elemental Impurities

ICH Q3 described expectations regarding the control of elemental impurities in medicinal products or their excipients. A control strategy should be implemented if the risk assessment shows that a source of elemental impurities exceeds 30% of the PDE limit.

Environmental Monitoring

We have invested in state-of-the-art equipment to perform active air sampling, as well as compressed gas sampling for microbiological assessment or non-viable particle counting.

Method Development

Method development and validation are essential to the drug development process to ensure the methods are well-defined and fit-for-purpose, and the results are robust and reliable.

Method Validation

To ensure that the methods meet regulatory requirements, we follow relevant ICH guidelines such as ICH Q2(R1) or compendial guidelines in combination with client-specific protocols.

Microbiological Services

We can support you with routine testing and validation of the microbiological purity of raw materials and finished medicinal products.

QC Chemical Analysis

Our GP certified QC laboratory can support your analytical needs from pharmacopoeial analysis of raw materials, active pharmaceutical ingredients (APIs), and investigational medicinal products (IMPs) to finished medicinal products.

QP Batch Release

Our Lab Services have authorization for testing and release of medicinal products in accordance with EMA Directive 2001/83/EC. Our own qualified persons (QPs) can certify the batch release testing.

R&D Projects

QbD Group's Lab Services is uniquely positioned to provide knowledge and customized solutions for the pharma industry.

Residual Solvent Testing (GC)

Reliable GMP-aligned residual solvent testing (GC) for APIs and finished products, ensuring compliance and patient safety.

Stability Studies

Investigating the stability and shelf-life of a finished product is an important area of expertise at QbD Group's Lab Services. We can help you determine the best approach for investigating the stability of your product with ICH stability testing.

Why QbD Group

Your trusted partner

QbD Group's Lab Services combines over 25 years of analytical expertise with a client-first approach. Our GMP-compliant laboratory delivers precision, reliability, and speed for all your pharmaceutical testing needs.

+25 years of analytical experience

deep knowledge across pharmaceutical testing methods and regulatory standards.

Tailored solutions

we adapt our services to your specific needs, whether you're a startup or a multinational.

Global reach

our lab serves clients across Europe with consistent quality and compliance.

Commitment to quality

state-of-the-art equipment and GMP conditions ensure reliable, accurate results every time.

Let's talk Lab Services

From method validation to stability testing, our lab experts are ready to support your analytical needs.