FDA-compliant, cGMP-approved dry ice cleaning for pharmaceutical manufacturing, cleanrooms, medical device facilities, and healthcare operations across South Florida. Zero moisture, zero residue, zero contamination risk.
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Specialized cleaning for every type of pharmaceutical and medical facility
Tablet presses, coating equipment, granulators, blenders, and packaging lines. Clean to cGMP standards without introducing moisture or chemical residues that compromise product quality.
ISO 5, ISO 7, and ISO 8 cleanroom cleaning including walls, ceilings, floors, and HVAC systems. Maintain sterile environments without water or particles that compromise classification.
Lab equipment, fume hoods, biosafety cabinets, and analytical instruments. Non-conductive cleaning safe for sensitive electronics and precision equipment.
Injection molding equipment, assembly lines, sterilization equipment, and packaging systems. FDA-compliant cleaning for Class I, II, and III medical devices.
Operating rooms, imaging equipment, HVAC systems, and facility infrastructure. Eliminate pathogens and maintain infection control without harsh chemicals.
Compounding equipment, laminar flow hoods, and preparation areas. USP 797/800 compliant cleaning for sterile and non-sterile compounding facilities.
Common problems facing pharmaceutical and medical facilities and how dry ice cleaning solves them
Traditional cleaning problem
Residue-free cleaning maintains ISO classifications without introducing particles, moisture, or chemicals. Clean validated equipment without revalidation requirements.
Avoid costly revalidation and maintain production schedules
Traditional cleaning problem
FDA-recognized cleaning method with complete documentation. No chemical residues, no moisture introduction, no cross-contamination risk between product batches.
Pass FDA inspections and maintain regulatory compliance
Traditional cleaning problem
Clean equipment in place without disassembly or cooldown. No drying time means immediate return to production. Reduce cleaning validation time by 70%.
Reduce downtime costs by $250K-$2M+ annually
Traditional cleaning problem
Eliminate biofilms, endotoxins, and microbial contamination without water that promotes bacterial growth. Maintain sterile manufacturing environments.
Prevent batch failures and product recalls
Proven benefits for regulatory compliance and sterile manufacturing
Explore our specialized services for pharmaceutical and medical facilities
Common questions from pharmaceutical and medical facility managers
FDA and cGMP-compliant cleaning solutions for pharmaceutical and medical facilities across South Florida
Serving pharmaceutical facilities across South Florida • FDA & cGMP compliant • Zero contamination risk