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CDMOs and Multimodal Facilities Cleanroom Cleaning
In contract development and multimodal facilities, the demands never stay the same for long. One week, you’re onboarding a new sponsor with unique standard operating procedures. The next week, you’re switching from cell and gene therapy to biologics or sterile fills.
Shared suites, shifting schedules, and parallel client expectations create constant pressure. Without a structured program, small variations in execution grow into serious problems. Cleaning steps get missed, documentation trails break down, and critical turnover timelines slip, leaving suites idle and sponsors frustrated.
That is where we step in. We build harmonized programs that adapt to different sponsor requirements, protect modalities, and deliver documentation that satisfies both your quality process and sponsor audits.
The Problems We Solve
- What it looks like
Competing standard operating procedures, different disinfectant lists, and uncertain changeover rules can cause teams to hesitate or miss key steps.
- How we prevent itWe stabilize this by creating a harmonized master program with client-specific addenda, clear changeover playbooks, and a crosswalk that maps every step to sponsor requirements.
- What it looks like
Idle time between campaigns, late starts, and finger-pointing are common when rooms are not released on time.
- How we prevent itOur approach uses turnover timers, pre-staged kits, segregated tools and consumables, and in-room verification before release. This keeps suites productive and campaigns on schedule.
- What it looks like
Missing signatures, multiple versions of logs, and long review cycles can derail audits.
- How we prevent itWe provide client-tagged room logs, technician training records, and summary packets that align with both sponsor expectations and your quality assurance process.
- What it looks like
When demand spikes or drops, internal staffing models struggle. Onboarding delays, inconsistent training, and unpredictable quality slips put programs at risk.
- How we prevent itOur solution is recurring trained crews, on-site supervision, and a staffing plan that flexes with your campaign calendar.
- What it looks like
Switching between modalities without strict controls can lead to contamination carryover of materials and tools, unclear line clearance, or chemistry incompatibilities.
- How we prevent itWe prevent this with strict segregation, color coding, verified contact times, residue management, and sign-off tied to your environmental monitoring plan.
Where We Support
Contract Development and Manufacturing Organizations (CDMOs)
CDMOs face sponsor-specific requirements, rapid technology transfer, and parallel client work
We design a site-wide core program with sponsor-specific overlays, client-named documentation packets, and turnover playbooks that protect your schedules and keep audits moving.
Multimodal Facilities
Shifting between cell and gene therapy, biologics, and sterile fills can undermine control if the program is not precise
We deploy dedicated tool sets for each production stream, disinfectant rotations tailored to surfaces, and clear zoning practices to ensure teams move correctly in mixed-use buildings.
What’s In It For You
One core program, many sponsors.
A harmonized site program with client-specific addenda, so teams don’t have to relearn basics for each sponsor.
Predictable room turnover.
Ready-to-use cleaning kits staged for each suite and client requirement segregated tools, and turnover timers that reduce idle time between campaigns.
Sponsor-ready documentation.
Client-tagged logs, technician matrices, and summary packets aligned with your quality process.
Capacity that flexes with the calendar.
Recurring crews, on-site supervision, and a staffing plan tied to actual campaign load.
Cross-platform protection.
Dedicated tools and chemistries, clear zoning, and residue control for safe transitions between treatment types such as cell and gene therapy, biologics, and sterile fills.
Audit-Ready Documentation
Sponsor-tagged room logs
Technician training records tied to your site
Sponsor-specific crosswalks to procedures
Deviation notes with corrective action handoff
Inspection readiness checklist aligned with sponsor and QA expectations
Proof In Practice
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.