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Analytical science for pharmaceutical development.

Brightlabs supports pharmaceutical organizations with method development, validation, quality control, stability studies, and specialized impurity analysis.

Pharmaceutical data must be accurate. Always.

In pharmaceutical development, the quality of your analytical data determines the certainty of every subsequent decision, from formulation to regulatory submission. A failing method, an overlooked impurity, or a stability risk discovered too late can delay a program by months. Brightlabs provides the analytical rigor to identify and manage these risks in a timely manner.

GMP

Fully accredited GMP laboratory

2015

Active in the pharmaceutical sector since our inception

Full lifecycle

From early development to commercial release

How we support pharmaceutical organizations.

Method Development & Validation

We develop and validate analytical methods from the ground up, designed for your specific compound, matrix, and regulatory context. From day one, we ensure compliance with the relevant guidelines of the International Council for Harmonisation (ICH) of Technical Requirements for Pharmaceuticals for Human Use.

Impurity Analysis

Identifying and quantifying impurities requires sensitive methods and scientific interpretation. We combine sensitive analytical techniques with scientific expertise.

Nitrosamine Analysis

As regulatory focus on nitrosamine impurities intensifies, we provide the validated methods and analytical sensitivity required for reliable compliance.

Elemental impurities

ICP-MS-based testing for elemental impurities in line with ICH Q3D—accurate, sensitive, and fully documented for regulatory submissions.

QC release testing

GMP-compliant QC testing with reliable turnaround times and full traceability, ensuring your release decisions are always based on data you can defend.

Stability Studies

We design stability programs that provide valuable and regulatory-compliant insights into shelf life and degradation at every stage of development.

The right technique for every challenge.

We apply a wide range of analytical techniques, always selected based on the complexity and regulatory context of the request.

HPLC
GC
LC-MS / LC-MS/MS
GC-MS / GC-MS/MS
ICP-MS
IC
UV/Vis
Headspace GC

Nitrosamine analysis

Brightlabs develops advanced analytical methods for the detection of nitrosamines and API-specific nitrosamine impurities (NDSRIs), enabling pharmaceutical organizations to comply with stringent regulations.

Impurity Analysis

Impurities often determine the difference between an approved and a rejected product. We bring them into focus.

Stability studies

Stability studies answer a question required by every regulatory dossier: how does your product behave over time?

QC Testing

QC testing is not a formality. It is the final, decisive check before a product reaches the market.

Method development

Method development is not a 'nice-to-have'. It is the foundation upon which everything else depends.

Analytical Troubleshooting

A method that worked for years but now produces inexplicable results is one of the most frustrating analytical problems. We solve them.

Science is only as good as the people behind it.

Brightlabs was founded on a simple belief: that analytical chemistry is most valuable when driven by genuine scientific curiosity and a commitment to doing things the right way.

Insights from our laboratory

Innovation for Health

Jeroen Wijker and Figo Seelen are on site speaking with companies that are pushing new therapies, technologies, and products forward.

Brightlabs appoints COO

Today, we are pleased to announce the strengthening of our team with the appointment of Dr. Sander Kok as Chief Operating Officer.

Put the soil to work for resilient crops

Brightlabs and Soil Vision have jointly developed a smart analysis method that reveals how soil life functions and how you can optimize it.

A pharmaceutical analytical challenge?

Talk to one of our scientists. We will help you determine the right analytical approach for your specific situation.