Services

Testing, maintenance, and validation support — in one place.

Four service lines built around one goal: controlled environments and systems your quality team can stand behind. Use them individually, or together when a project touches more than one.

Cleanroom & contamination-control testing

Testing and reporting that support classification, monitoring, and contamination-control decisions.

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Typical scope

HEPA integrity · smoke studies · particle counts · room performance checks · EM program support

When teams call us

New suite nearing qualification; requalification due; HVAC or filter changes; EM trends

Derouging & passivation

Stainless process-system care, planned around your downtime and documented for your quality file.

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Typical scope

Assessment · derouging · passivation · post-install passivation · verification records

When teams call us

Visible rouge; new install or modification; planned shutdown

CQV, engineering & project management

Commissioning, qualification, and validation support sized for small and mid-size projects.

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Typical scope

C&Q plans · IQ/OQ/PQ · turnover review · project coordination · readiness reviews

When teams call us

First GMP suite; expansion; new equipment or utilities; process change

Computer system validation

Risk-based validation support for the systems behind your GMP records.

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Typical scope

Validation plans · URS & risk · supplier assessment · testing · periodic review

When teams call us

New LIMS/MES/eQMS; software upgrade; data-integrity findings

Why one partner helps.

A facility's readiness story is spread across test reports, maintenance records, protocols, and system validation. When those come from one team, formats match, references line up, and there's one place to ask questions. You still choose exactly which services you need.

  • Testing data
  • Stainless records
  • CQV protocols & reports
  • CSV evidence
  • Your facility-readiness record

Questions we hear often

Do you take on single projects or ongoing programs?

Both. Recurring testing and monitoring support suit ongoing programs; CQV and CSV work is usually project-based. Many clients start with one and add the other as needs come up.

Can you work with our SOPs and templates?

Yes — that's our preference. Where your quality system has templates and acceptance criteria, we use them. Where it doesn't, we propose formats for your QA team to review and approve.

Do you guarantee inspection or audit outcomes?

No one can honestly do that. What we provide is well-planned work and clear, reviewable documentation. Acceptance decisions stay with your quality unit.

Where do you work?

We serve facilities across North Carolina, primarily in the Research Triangle — RTP, Durham, Raleigh, Chapel Hill, Morrisville, Holly Springs, and nearby.

How do we get started?

Send a note through the contact form. We'll set up a short scoping conversation and follow with a written scope.

Planning a new suite, an expansion, or a recurring test program?

Tell us what you're working on. We'll reply with a few questions, a suggested scope, and next steps.

Request a facility-readiness conversation