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

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

Custom Decontamination Services

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

Controlled Environment Disinfection

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

Specialized Service Packages

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

Audit & Compliance Support

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

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Cleanroom Cleaning & Disinfection Solutions

Cleanroom Cleaning & Disinfection Solutions

We design cleanroom cleaning and disinfection programs that keep your production running smoothly. Every program delivers standardized execution, traceable records, and access windows that respect your schedules.
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Why Cleanroom Cleaning & Disinfection Is Critical

In regulated environments, cleaning is a core operation that directly impacts production release, product yield, and audit readiness. When methods drift, tools vary between shifts, or logs fail to tell the complete story, confidence is lost. Quality teams lose trust, Operations lose valuable time, and inspections slow down.

Our cleanroom cleaning and disinfection solutions replace ad-hoc efforts with a structured system: trained technicians, process-validated methods, and Good Documentation Practice (GDP) records that work across rooms and sites.

Who We Serve

Every function feels the effects of cleaning variability differently, but all benefit from consistency and traceability.

Operations get predictable access windows, fewer interruptions, and optimized production flow.

QA and Regulatory get consistent execution, room-level traceability, and inspection-ready record packs.

Engineering and Facilities get methods compatible with sur
faces and equipment, supported by clean change control.

Procurement and Finance get scoped SLAs, leveled hours, and scalable programs across sites.

What to Expect

At Vibraclean, cleanroom cleaning is not a task but a program designed to build lasting stability.
We begin by reviewing your Standard Operating Procedures (SOPs), contamination control strategy, material and personnel flows, environmental monitoring trends, and operational constraints. The result is a site playbook and risk register that anchor the program.
Once calibrated, trained technicians follow the plan using segregated tools, colour coding by class and zone, verified contact times, and GDP-compliant room logs.
We run the method in a limited set of rooms to fine-tune cadence, crew size, dwell verification, and hand-offs, while avoiding bottlenecks in production.
Agreed review cycles track findings from EM data, rework, and access conflicts. Small, approved changes are introduced through your change-control process, ensuring the program remains stable and continuously improves.

The Pillars We Build On

Our programs are built on four pillars that give you confidence and consistency.

Standardization

Room and class-based methods, controlled tools, verified dwell times, and documented line clearance during changeovers.

Traceability

GDP records mapped to rooms, shifts, chemistries, and acceptance criteria, retrievable in seconds.

Regulatory Fit

Alignment with cGMP, EU-GMP Annex 1, ISO 14644, and your CCS. Our teams train to your SOPs and document to your templates.

Operational Continuity

Access windows are planned with Operations so cleaning protects campaigns and studies rather than interrupting them.

What Sets Us Apart

Unlike many providers, our technicians are not only trained to regulatory standards but also backed by an internal Quality Assurance department that actively oversees their work.
This dual layer of regulatory training plus QA oversight ensures:
  • Every step withstands audit scrutiny.
  • Records meet the highest compliance standards.
  • Consistency across shifts, rooms, and sites.
It is a safeguard that few competitors offer, and it is why clients trust us when inspection readiness and operational continuity are at stake.

The Value of Cleanroom Cleaning & Disinfection

Vibraclean brings clarity and consistency to some of the most common cleanroom challenges:

Multi-room or multi-site
facilities.  Where every area needs to follow the same methods and keep records that align across locations.

Teams stretched thin where scientists or associates are still pulled into end-of-shift cleaning. We step in so their time stays focused on production and research.

Sites struggling with recurring problems caused by inconsistent cleaning or incomplete documentation. Our structured methods and clear records help restore compliance and confidence.

With Vibraclean, what once caused delays, rework, or stress during inspections becomes a stable, reliable part of operations.

What You Receive With Our Solutions

Our solutions make the biggest impact in environments where consistency and compliance are at risk:

A Site Playbook with methods by room/class, tools, chemistries, dwell times, and acceptance criteria.

A Training Matrix and Competency Sign-Offs for every assigned technician.

Room-Level Logs (GDP-compliant) cross-referenced to your SOPs and CCS

An Access Plan synchronized with Operations, including escalation paths for exceptions.

Regular Review Cycles aligned to your KPIs, ensuring performance trends are tracked and improvements introduced at the right pace.

Audit-Ready Documentation

Room and shift release logs

Technician training records

Procedure crosswalks

Deviation notes with corrective and preventive
action handoff

Inspection readiness checklist tied to environmental monitoring and radiation safety requirements

Proof in Practice

One hospital pharmacy struggled with persistent residue on shields and pass-throughs. 
We introduced adjusted chemistries, implemented a simple wipe sequence, and trained a recurring team. Within weeks, follow-up checks confirmed clear surfaces, and documentation reviews moved faster with fewer quality comments.

Tailored Solutions

Custom cleaning and disinfection programs designed for your facility’s unique compliance needs.

25+ Years Expertise

Decades of proven experience delivering critical disinfection across regulated industries.

10+ Years Research

Extensive particle and bio-burden control expertise across multiple industries.

Proof In Practice

The impact of our cleanroom cleaning and disinfection solutions is clear. Facilities see fewer cleaning-related issues, smoother inspections, and more productive hours for their internal specialists. Records are retrieved faster, with fewer clarifications needed. Internal specialists gain more productive hours. Costs stabilize without end-of-month labour spikes.

Most importantly, your teams stop scrambling and start working with confidence, knowing they are always ready for inspection day.

Tailored Solutions

Custom cleaning and disinfection programs designed for your facility’s unique compliance needs.

25+ Years Expertise

Decades of proven experience delivering critical disinfection across regulated industries.

10+ Years Research

Extensive particle and bio-burden control expertise across multiple industries.

Get Started With Precision Cleanroom
Cleaning & Disinfection.

Getting started is simple. Talk with our experts about the challenges you are facing today or the risks you want to get ahead of tomorrow. We will design a program that delivers stability, compliance, and confidence without disrupting production.

Talk to a Cleanroom Specialist