ProCleanCorp delivers TGA/GMP-aligned sterile cleaning for cleanrooms, pharmaceutical facilities, medical device environments and research laboratories across Sydney — with documented SOPs and validated cleaning agents.
✓ TGA/GMP Compliant | ✓ ISO Cleanroom Standards | ✓ Documented SOPs
Sterile cleaning is distinct from standard medical cleaning — it requires validated cleaning agents, documented SOPs, classified PPE and protocols verified against ISO 14644 cleanroom standards or TGA/GMP guidelines. ProCleanCorp provides specialist sterile cleaning for cleanrooms, laboratories, pharmaceutical manufacturing and medical device facilities across Sydney, with cleaning logs maintained for TGA audit readiness.
In cleanroom, laboratory and pharmaceutical environments, cleaning is not simply about hygiene — it is a critical quality control process. A contamination event caused by incorrect cleaning can compromise batch integrity, invalidate research results, or trigger a TGA regulatory action. ProCleanCorp's sterile cleaning teams are trained in contamination control principles, use validated cleaning agents and maintain documentation to the standard your quality system requires.
Our cleaning SOPs are developed in collaboration with your quality assurance team, not imposed from outside. We understand that each facility has unique contamination control requirements — a pharmaceutical compounding cleanroom has different cleaning demands to a university research lab or a medical device packaging room — and we build the programme accordingly.
Pharmaceutical manufacturing, medical device packaging, electronics assembly
University labs, R&D facilities, pathology, molecular biology
Compounding pharmacies, manufacturing suites, QC labs
Device assembly, sterile packaging, testing suites
Cell culture rooms, fermentation facilities, analytical labs
CSSD support areas, sterile storage, prep rooms
Sporicidal, bactericidal and virucidal agents rotated to prevent adaptive resistance. Selected in consultation with your QA team.
All cleaning procedures documented in client-approved SOPs. Cleaning logs maintained for TGA audit readiness.
Staff trained in cleanroom gowning, contamination control procedures and GMP principles before any classified room entry.
Cleaning protocols designed to support the particle count requirements of ISO Class 7 and Class 8 environments.
Cleanroom and pharmaceutical cleaning is quoted after a site assessment and review of your contamination control requirements.
Standard medical cleaning (GP practices, specialist suites) targets infection control for clinical environments — hospital-grade disinfectants, colour-coded equipment, documented schedules. Sterile cleaning goes further: it is designed for controlled environments where even trace contamination can compromise product integrity or research outcomes. Sterile cleaning requires validated cleaning agents, documented SOPs, personnel in appropriate PPE, and cleaning protocols verified against ISO 14644 cleanroom standards or TGA/GMP guidelines.
Yes. ProCleanCorp provides GMP-aligned cleaning for pharmaceutical manufacturing, compounding pharmacies and medical device facilities in Sydney. Our cleaning SOPs are documented, our cleaning agents are validated (not just disinfectant-grade), and we maintain cleaning logs that satisfy TGA audit requirements. We work with your quality assurance team to ensure our cleaning programme integrates with your quality management system.
ProCleanCorp services ISO Class 7 and ISO Class 8 cleanrooms in research, manufacturing and pharmaceutical settings in Sydney. For ISO Class 5 and Class 6 environments, we work with the facility's contamination control officer to ensure our cleaning programme meets the specific particle count requirements for that classification. All cleaning in classified environments is conducted by staff with cleanroom entry training.
We use validated sporicidal, bactericidal and virucidal cleaning agents appropriate for the contamination control requirements of each environment. Agents are rotated to prevent adaptive resistance. All products used in pharmaceutical and cleanroom environments are selected in consultation with the client's QA team and documented in the cleaning SOP. We do not use fragrance or residue-leaving products in sterile environments.
Site assessment included. Cleaning programme developed with your QA team.