Accredited endotoxin testing services

From routine batch release to complex LER investigations, CMD provides UKAS-accredited endotoxin testing designed to support compliance, product development and manufacturing continuity

Find the right support for your endotoxin challenge

Different organisations require different levels of support. Whether you are implementing endotoxin testing for the first time, working within a defined budget or requiring accredited results for release, our service adapts to your regulatory and operational needs.

New to Endotoxin Testing?

If endotoxin testing is new to your organisation, we guide you through the process clearly and efficiently. From defining limits to understanding sample requirements, we ensure you meet regulatory expectations without unnecessary complexity.

Accredited Test Results Required?

When inspection readiness and documented traceability are essential, we provide UKAS-accredited endotoxin testing with structured reporting suitable for regulated pharmaceutical and biotech environments.

Limited Product or Budget?

For early-stage companies and low-volume manufacturers, outsourcing provides compliant testing without capital investment. Our service supports small batch sizes and development-stage products with transparent turnaround options.

Need Rapid Turnaround Testing?

Where timelines are critical, we offer defined turnaround options to support batch release and production continuity. Early technical review helps prevent delays caused by incomplete documentation or unsuitable samples.

Our Endotoxin Testing Services

Our laboratory operates under UKAS accreditation (No. 23137) and ISO 9001 certification, delivering validated, traceable and inspection-ready data.

    • Batch release testing

    • Raw materials and intermediates

    • Finished products

    • Purified water and dialysis fluids

    You receive structured reporting, defined turnaround timelines and technical follow-up where required.

    • Product-specific validation

    • Interference testing

    • Pharmacopoeial compliance alignment

    • Bridging support for internal transfer

    Designed for new products, reformulations and challenging matrices.

    • Structured recovery investigations

    • Controlled spiking studies

    • Data interpretation support

    • Regulatory-aligned reporting

    Supporting biologics and complex formulations.

    • Investigation of unexpected inhibition or enhancement

    • Support for out-of-specification results

    • Risk-based discussion of next steps