Home

Expertise

QC Testing

When quality is non-negotiable, we check every batch.

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

Every batch deserves the same precision as the first.

Routine quality control sounds simple, but the consistency it requires is anything but. Every batch must meet the same specifications, whether it is the first or the thousandth. Our QC testing combines qualified methods with the discipline of a GMP laboratory to guarantee that consistency.

QC testing is therefore relevant in every sector we serve.

Routine testing is not a matter of automation.

Reliable quality control requires more than just following a protocol. It requires sharpness, traceability, and the ability to recognize deviations before they become problems.

Consistency under pressure

Production schedules don't wait. QC testing must be fast and reliable, batch after batch, without compromising accuracy.

Traceability and documentation

Every result must be traceable to the method, instrument, and analyst used. Our GMP workflow makes every result audit-ready.

Early detection of deviations

An out-of-specification result is not an endpoint, but a signal. We identify trends and deviations before they escalate into production issues.

Expertise

Reliability

Flexibility

Partnership

From sample receipt to release decision.

Our QC workflow is designed to combine speed and accuracy, so you can release batches with confidence.

Sample receipt and registration

Every sample is registered with full traceability, origin, batch number, and the specifications against which it must be tested.

Analysis according to qualified method

We apply the method qualified for your product, using the appropriate controls and reference standards to ensure the accuracy of every result.

Evaluating results against specifications

Every result is checked against the established specifications. In the event of any deviations, we investigate the cause before reporting.

Documentation and reporting

Complete documentation of methods, results, and any deviations, ready for your quality file and any potential audits.

Support for release decisions

We provide more than just numbers; we provide context. In cases of doubt, we help you evaluate what the result means for the batch release.

Sectoren waar methodeontwikkeling essentieel is.

Farma

Nieuwe verbindingen, complexe formuleringen, generieke geneesmiddelen

Cannabis

Plantaardige matrices, innovatieve CBD-producten, niet-standaard extracten

Voeding

Innovatieve ingrediënten, bijproducten, niet-standaard matrices

Industry

Klantspecifieke verbindingen en industriële materialenerialen

Verder verkennen.

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?

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.

The complete overview of what Brightlabs does.

Download our brochure for a complete overview of our analytical capabilities, services, and scientific approach.