Contamination Control for Critical Life Science Environments

Specialized cleaning, decontamination, and compliance solutions for pharmaceutical, biotech, cleanroom, and healthcare facilities, delivered by certified technicians with deep GMP expertise.

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Why Sterile Science Matters

One Contaminant Can Compromise Your Entire Operation

In pharmaceutical manufacturing, biotech research, and healthcare environments, contamination isn't a housekeeping problem, it's a compliance failure, a patient safety risk, and an operational shutdown waiting to happen.

  • A single contamination event can void entire production batches, triggering costly recalls and regulatory action
  • Commercial cleaning companies lack the GMP protocols required for validated cleanroom environments
  • Environmental contamination directly threatens product integrity, patient outcomes, and FDA compliance
  • Post-construction decontamination is a mandatory prerequisite before any life-science facility can go live
  • Sterile Science delivers documented, audit-ready procedures, so your cleanroom is always inspection-ready

45+ Years of Experience
Supporting Mission-Critical Facilities

250+

Technicians

Fully trained technicians supporting ongoing maintenance programs in the field.

100+

Million Sq. Ft.

Critical environment experience delivered over the last 18 months.

Certified

ISO 9001 & 14001

Certified quality and environmental management systems.

Our Services

Precision Solutions for
Every Critical Environment

From routine cleanroom maintenance to high-risk bio-decontamination, our certified teams deliver results that hold up under the toughest regulatory scrutiny.

Cleanroom Cleaning

From routine ISO-compliant maintenance to deep super cleans and post-construction preparation, tailored to your protocols and classification requirements.

Dry Fog Sterilization

Rapid, validated disinfection achieving a 99.9999% (6-log) microbial kill rate using Minncare Dry Fog technology. Ideal for complex geometry with minimal contact time.

Bioburden Reduction

Manual cleaning, targeted disinfection, and contamination control planning using GMP-compliant techniques, validated products, and fully documented procedures.

Facility Disinfection

Full-facility sanitization programs covering cleanrooms, labs, warehouses, and common areas, using scientifically proven methods appropriate for each zone classification.

Technical Consulting

Expert environmental analysis, risk assessments, SOP development, and cleaning program design to help your team build and maintain best-in-class cleanroom practices.

Environmental Monitoring

Ongoing environmental sampling, trend analysis, and reporting to maintain compliant microbial and particle counts across your controlled environments.

Industries Served

Built for the Most
Regulated Environments

Sterile Science supports life science, pharmaceutical, biotech, and healthcare environments with contamination control services tailored to strict regulatory and operational protocols.

Pharmaceutical

GMP-compliant cleaning, bioburden reduction, validated products, and documented procedures for pharmaceutical and controlled cleanroom environments.

GMP-Compliant Validated Products Dry Fog

Biotechnology

Bioburden reduction, contamination control planning, and documented cleaning procedures for biotech and controlled cleanroom environments.

Bioburden Reduction Cleanroom Cleaning Documented Procedures

Healthcare & Medical Devices

Facility disinfection, decontamination, and contamination control support for healthcare and critical environments with strict cleanliness and safety requirements.

Facility Disinfection Decontamination Compliance Support

Advanced Manufacturing

Routine maintenance, deep cleaning, and post-construction preparation for critical cleanroom environments with documented cleanliness requirements.

Cleanroom Cleaning Routine Maintenance Post-Construction

Our Approach

Precision From Assessment to Documentation

Every project starts with a site-specific review and ends with clear documentation, helping teams maintain traceability, cleanliness standards, and alignment with internal protocols.

01

Site Assessment & Risk Mapping

We begin with site surveys, environmental analysis, and risk assessments to understand your facility, contamination concerns, and cleaning requirements.

02

Protocol & SOP Development

We help develop SOPs, cleaning programs, and documented procedures using validated products and methods aligned with your facility’s protocols and regulatory needs.

03

Certified Technician Execution

Trained technicians carry out the work using documented cleaning, disinfection, and contamination control methods appropriate for critical environments.

04

Audit-Ready Documentation

Work is supported by documented procedures and service records that help your team maintain internal traceability and regulatory preparedness.

Talk to a Sterile Science Expert

Your Environment Can't Afford the Wrong Partner

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Looking to speak to someone directly? Call 800-328-2256

Nationwide Coverage. 45+ Years of Experience.

Talk to a Promera Specialist About Your Facility

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