GMP Services

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Benefit from our specialised department for GMP-compliant cleaning, backed by a professional training program and a pharmaceutical-grade quality management system. Trust our trained personnel to deliver the highest quality standards and ensure maximum safety for the life sciences industry.

What we do for you

ISS runs your GMP cleaning operations end-to-end across classified and controlled areas — fully integrated with your PQMS. We design routines, train and qualify teams, provide validated materials, and document every clean so you stay audit-ready.

  • Cleaning of GMP or ISO 14644 classified areas and supporting areas

  • Daily/weekly routines, campaign & changeover cleans

  • SOP-linked records & traceability

  • Role-based training & effectiveness checks

  • Validated single-use/reusable materials

  • Deviation, CAPA & change control interfaces

Result: stable environments, predictable compliance, and less production downtime during changeovers and shutdowns.

ROLE-BASED TRAINING

Audit-ready Records

GMP/GDP PQMS

What we deliver

A modular service catalogue that you can combine into the operating model you need.

  • Validated routines for classified and controlled areas, including rooms, airlocks, material flows, and support spaces.

    • Floors, walls, ceilings; fixtures & exteriors

    • Material/personnel airlocks & gowning

    • Zoning (e.g., Grade-based routines)

    • Cleaning after alterations or zone shutdown

  • SOP-linked records, logbooks, checklists, and electronic evidence aligned to site PQMS.

    • SOP-linked records & logbooks

    • Cleaning maps & frequencies

    • Material & consumable traceability

    • Deviation & change control interfaces

  • Role-based curricula, refreshers, effectiveness checks, and ongoing competency management.

    • Role-based curricula & refreshers

    • Read & understand + practical checks

    • Supervisory QA walkthroughs

    • HSE & gowning compliance

  • Change control integration, deviation reporting, root-cause, and corrective actions.

  • Support to EM routines (e.g., surface/contact plates handling and area prep) as defined by your QA.

  • Planned cleaning for changeovers and shutdowns with controlled re-entry and documentation.

Packages

Choose a package—or mix & match—to fit your facility and risk profile.

CORE

  • Controlled areas (non-classified)

  • SOP-driven daily/weekly cleaning

  • Paper logbooks & checklists

  • Standard training & onboarding

CLEANROOM

  • Classified cleanrooms & airlocks

  • Zoning & material flow control

  • SOP-linked records & traceability

  • Supervisor QA walkthroughs

eNHANCED

  • Campaign/changeover programs

  • Electronic logs & KPI dashboards

  • Deviation/CAPA integration

  • Audit preparation support

Talk to our Gmp sERVICES experts

Share your lab footprint and priorities. We respond within one business day.

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