Modern sterilization for

medical niche production

Your trusted partner in medical compliance

At Sterillab, we offer to bridge the gap between high-standard pharmaceutical and medical requirements and the need for flexible, small-batch production. While many laboratories prioritize mass production, we have dedicated our facility to the specialized sterilization of small-volume glassware and pipettes for pharmaceutical companies and research institutions.

Modern facilities – Documented quality

We have recently completed a total upgrade of our sterilization equipment, ensuring that our clients in Denmark, and across Europe benefit from the latest advancements in sterilization technology. Our processes are designed for agility without ever compromising on the rigorous safety standards required by the medical industry.

Sterilization-as-a-Service and ready-to-fill

With 50+ years legacy, Sterillab delivers validated sterilization, ready-to-use primary packaging directly to your filling lines. Discover our turnkey, multi-component dropper system with high-durability, shock-resistant Type 1 amber glass vials integrated with child-resistant pipette assemblies including a mounting system.

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Uncompromising Quality & Technical Excellence

Our commitment to compliance ensures that your niche production meets the highest global standards.

1. GMP standards & methodology

The foundation of our production standard

We operate with strict adherence to Good Manufacturing Practice (GMP). This ensures that every step of our washing and sterilization processes are documented, validated, and repeatable, giving you the necessary confidence in our pharmaceutical-grade production.

2. ISO Certified Excellence

Dual certification: ISO 9001 & ISO 15378

Sterillab is proud to maintain dual certification. ISO 9001 guarantees our quality management, while ISO 15378 specifically addresses primary packaging materials for medical products. This specialized certification reflects our expertise in handling glassware and plastic bottles for the pharmaceutical industry.

View our Certificates & Compliance

3. Controlled AB environment

Advanced cleanroom operations

Highest level of quality requires control. We operate within Grade A and B environments (AB), ensuring that your products are handled in highly regulated zones. Our facility is designed to meet the strict requirements for aseptic processing and sterile product handling.

Explore our Facility & Cleanrooms

4. Ultra-Low particle pressure

Minimized contamination risk

Our state-of-the-art ventilation systems and monitoring ensure an exceptionally low particle count in our production rooms. By maintaining superior air quality and environmental control, we safeguard the integrity of your small and mid-sized batches.

Discover our Technology & Quality Control

Advanced Depyrogenation & dry heat sterilization

Our state-of-the-art depyrogenation oven ensures the complete elimination of microorganisms and pyrogens through meticulously controlled thermal cycles.

To guarantee absolute consistency and compliance, the sterilization effect is monitored and documented in real-time via integrated PLC technology, utilizing precise F-value calculationsfor every batch.

Advanced Autoclave processing

We offer high-precision, fully validated steam sterilization solutions designed to meet the rigorous demands of the pharmaceutical and medical industries.

Our advanced autoclave systems provide versatile cycle configurations, including pulse pre-vacuum, gravity, and air-over-pressure, ensuring optimal heat penetration and stability.

Validated WFI Rinsing & Bioburden reduction

A critical prerequisite for successful sterilization is the removal of contaminants at the earliest stage.

By integrating WFI rinsing into our workflow, we provide a seamless "ready-to-sterilize" solution that safeguards the integrity of small and mid-sized batches from start to finish.

Eliminate Bioburden & Endotoxins
Remove Particulates