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Pharma and Biotech Cleanroom Cleaning
We solve the problems that put your batches, compliance, and schedules at risk.
The Problems We Solve
In pharmaceutical and biotech production, even minor cross-contamination can compromise an entire campaign. Material mix-ups, tool carryover, and disinfectant rotation drift are common risks that can create confusion during line clearance.
To prevent this, we implement campaign playbooks, segregated tools and carts, and colour coding. Verified contact times and pre- and post-clean checks are tied directly to your environmental monitoring plan, ensuring every changeover is consistent and fully documented.
When cleaning execution varies from shift to shift, results can be unpredictable.
Workstations may fail visual inspection, cleaning sequences may differ in similar suites, and rework often delays production.
We prevent this through room-specific work instructions, trained recurring teams, on-site supervision, and completion checks at the door. With these safeguards in place, cleaning results remain consistent no matter the room or shift.
Missing initials, unclear timestamps, vague annotations, and logs that fail to align with your standard operating procedures create unnecessary inspection delays.
Our teams close those gaps with room-level logs that detail who performed each task, when it was done, and the results achieved. A crosswalk maps every step to your standard operating procedures, while a summary supports your quality assurance review.
Residue, hazing, or corrosion on surfaces can interfere with environmental monitoring and equipment performance. Hazing on acrylic or corrosion on stainless steel are common examples.
To protect surfaces and maintain compliance, we work only with pre-approved chemistries, structured rotation plans, residue management steps, and material compatibility checks.
When suites are held out of service after a deviation or construction project, the entire production schedule suffers.
Our rapid decontamination projects follow defined timelines with traceable records and coordinated quality assurance sign-off.
The result is a controlled return to service that keeps production on track.
During start-ups, temporary fixes, unclear roles, and confusion during the first inspection often put new programs at risk.
We support these transitions with on-site training, pilot sequences, and repeatable programs that scale easily.
From the first inspection onward, your program is reliable and audit-ready.
Where We Support Pharma and Biotech
Monoclonal Antibodies
Cross-contamination between campaigns, complex change parts, and long runs that drift from the plan are common challenges.
We address them with strict campaign changeover playbooks, segregated consumables, contact time verification, and line clearance checklists tied to your environmental monitoring sampling plan.
Vaccine Production
Aseptic intervention risk, isolator residues, and time pressure between batches can disrupt vaccine production.
Our approach includes Grade B and Grade A friendly sequences, isolator cleaning both inside and out, material air lock wipe-downs, equipment touchpoint routines, and detailed batch record notes to support faster quality assurance reviews.
Cell and Gene Therapy
Small batch variability and autologous workflows demand precision. Isolator and biological safety cabinet sequences must be exact.
We provide suite-specific standard operating procedures, high-frequency changeover support, strict material and waste flow, and chemistries designed for sensitive cell work and surfaces.
Sterile Manufacturing
In sterile manufacturing, unclear roles between critical and background areas, disinfectant rotation drift, and residue on vision panels or equipment can undermine Good Manufacturing Practice expectations.
We clarify roles for critical and background areas, maintain rotation plans with documented contact times, manage residues on stainless steel and acrylic, and align processes with regulatory requirements.
Injectables
Line clearance delays, contamination risks with changing parts, and incomplete documentation create risk for injectable production.
We support operations with pre-fill line preparation, change parts staging and wipe down, between-lot line clearance, post-fill sanitization, and batch record-friendly documentation.
Viral Vectors
Bioburden spikes during campaigns, spill response in negative pressure rooms, and polymer damage from harsh chemistries can stall viral vector programs.
Our teams establish vector suite zoning habits, provide targeted decontamination for spills and campaign closeout, and perform compatibility checks to protect polymers and equipment.
What’s In It for You
Routine Cleanroom Cleaning Programs
We deliver daily, weekly, and campaign-based cleaning schedules that match your shifts.
Each team arrives fully trained with room-specific instructions, approved tools, and detailed checklists. Supervisors verify completion inside the room, so any issues are resolved before handoff.
Start-Up and Change Control Support
New rooms, expansions, and product changeovers require careful coordination. We refine your standard operating procedures where needed, provide on-site training, and run pilots until each step is correct.
Your program is inspection-ready on day one and easy to repeat on day two.
Rapid Decontamination
When contamination or construction halts production, time is critical.
We mobilize an expert-validated team with the right chemistries, coordinate with your environmental monitoring lead, document contact times, capture results, and return rooms to service on an agreed-upon timeline.
Program Consulting
A strong, documented program should outlast any single project team.
We review people flow, material flow, chemical selection, tool strategy, and staffing. We also design training, competency checks, and routine audits that your team can own long-term.
Audit-Ready Documentation
Room-level logs with who, what, when, and result
Technician training records
A Crosswalk mapping our steps to your standard operating procedures with flagged updates
Deviation notes, including root cause, corrective action, and handoff to your CAPA process
Inspection readiness checklist tied to
your environmental monitoring approach
Proof In Practice
Tailored Solutions
Custom cleaning and disinfection programs designed for your facility’s unique compliance needs.
Technician training records
Training records for every technician assigned to your site
Procedure crosswalks
Extensive particle and bio-burden control expertise across multiple industries.