Our validated cleaning programs protect batches and operations. Defined rotations, contact times, and in-room verification keep production on schedule with audit-ready records.
We harmonize sponsor-ready programs across modalities and shared suites. Clear changeovers and traceable documentation reduce idle time and keep campaigns moving.
We support sterile and non-sterile compounding with standards-aligned workflows. Segregated tools, defined rotations, and verification enable safe release and clear records.
We service hot labs and production suites with shield-friendly methods. Targeted cleaning, rapid turnarounds, and clear documentation keep time-sensitive work on track.
We build flexible programs around experiments and instrument schedules. Routine upkeep and one-time resets protect equipment and provide documentation for QA and sponsors.

Our validated cleaning programs ensure consistency, traceability, and compliance in every room, shift, and site, maintaining production on schedule.

We design and validate organism-specific decontamination programs that restore operations safely and withstand regulatory scrutiny.

From contamination incidents to shutdown recovery, our decontamination teams deliver validated results and complete regulatory documentation.

We build specialized service packages aligned to your production schedule — minimizing disruption, stabilizing costs, and ensuring audit-ready results.

We strengthen contamination control programs with aligned systems, clear records, and trained teams, so every inspection runs smoothly.

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Decontamination Technologies for Emergency Response

In critical environments like cleanrooms, an unexpected contamination event can jeopardize operations, compliance, and product integrity. Decontamination technologies designed for emergency response play a vital role in quickly neutralizing contaminants, restoring cleanroom conditions, and minimizing downtime. This blog explores the advanced decontamination solutions available for cleanrooms facing emergency scenarios. The Importance of Rapid Response in […]

Critical Environment Decontamination: Beyond the Basics

In industries where sterility is paramount, such as pharmaceuticals, biotechnology, and semiconductor manufacturing, critical environment decontamination is essential. This process involves the removal of contaminants that could potentially compromise product quality and safety. Vibraclean utilizes advanced decontamination techniques to ensure these environments meet the highest standards of cleanliness. Decontamination Methods Decontamination in critical environments involves […]

Overview of Hydrogen Peroxide Fogging

What Is Disinfectant Fogging? Fogging is a better choice for facility sterilization. It can eliminate all of the contaminants in your cleanroom, even the ones that are buried in hard-to-reach spots — between the floorboards, behind cabinets, or in the cracks between a row of desks. How Does Disinfectant Fogging Work? Disinfectant fogging starts with […]

How to use and validate iHP® Cycles

Ionized Hydrogen Peroxide (iHP®) iHP® is hydrogen peroxide, which is split into reactive oxygen species (ROS) by Binary Ionization Technology (BIT), increasing its efficacy and effectiveness as a disinfectant. iHP® is also classified as a sterilant, meaning that it can achieve sterilization of a surface, material, or room. As a sterilant, it can eradicate all […]

Choosing the Right Decontamination Method for Your Facility

Cleanroom decontamination isn’t one method fits all. The right approach depends on several variables: the type of facility, the classification level, the product being manufactured, the type of contamination, and the materials and equipment within the environment. Choosing the wrong method can lead to incomplete sterilization, damage to sensitive systems, or unnecessary downtime. At Vibraclean, […]