Lab & Cleanroom Care

Contamination-controlled cleaning around sensitive instrumentation, sample integrity, and cleanroom classifications.

What we do

How this service works.

Cleanrooms fail on invisible details. Our crews are trained on gowning, wipe patterns, and what NOT to touch — and we document every visit.

Our process

How we take on your facility.

  1. 01

    Classification & scope

    We confirm the ISO class of every room and write a protocol that matches — gowning, consumables, wipe pattern, and frequency all mapped to classification.

  2. 02

    Gowning & entry protocol

    Crews follow your gowning SOP — coveralls, hoods, boots, gloves — and enter through your airlock exactly like your staff does.

  3. 03

    Class-appropriate consumables

    Sterile, low-particulate, static-controlled wipes and mops sized to the ISO class. No consumable enters the room that shouldn't be there.

  4. 04

    Documented wipe patterns

    Ceiling to floor, clean to dirty, unidirectional strokes — the pattern is trained, supervised, and logged for every visit.

  5. 05

    Particulate & compliance logs

    Visit logs, consumable lot numbers, and gowning records ready for your quality team's audit — no scramble at survey time.

Standards & compliance

Built to the codes your team is audited on.

  • ISO 14644 cleanroom classification
  • USP <797> / <800> aware protocols
  • cGMP-supportive cleaning practices
  • OSHA general industry compliance
  • Static-controlled, low-particulate consumables
Facilities we serve

Environments we know cold.

  • Research & academic labs
  • Biotech & pharma cleanrooms
  • Medical device manufacturing
  • Semiconductor & electronics
  • Compounding pharmacies
  • Analytical & QC labs
FAQ

Answers before you ask.

Do you work in ISO Class 5 / 7 / 8 environments?
Yes. Protocol, consumables, and gowning scale to classification — we confirm the class per room during scoping and match everything to it.
How do you avoid disturbing sensitive equipment?
Crews are trained on a do-not-touch map for every room. Instruments, samples, and open work areas are documented up front and worked around, never over.
What consumables do you use?
Sterile, low-particulate, static-controlled wipes and mops — with lot numbers logged per visit for your quality file.
Can you support cGMP or USP audits?
Yes. Visit logs, consumable lot numbers, training records, and gowning documentation are kept per room and produced on request.
Do you train around our SOPs?
Always. We work to your gowning, entry, and cleaning SOPs — we don't overwrite them with ours.
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