Spec Services Commercial have experience in cleaning to ISO 5 clean room specifications including testing air cleanliness and continued verification of the cleaning itself. We understand the requirement of a validated, well-documented cleaning and sanitization process for the equipment a space used for manufacturing and laboratory clean rooms.

Cleaning is an important process step in the field of production. Spec Services prescribe to the GMP-compliant cleaning P’s – people, premises, processes, products and procedures (or paperwork).

Cleaning and sanitation of premises and equipment are essential to efforts to prevent contamination of product, and they need to be done in compliance with Good Manufacturing Practice (GMP) regulatory requirements.

Cleaning validation is the methodology used to assure that a cleaning process removes chemical and microbial residues of the active, inactive, or detergent ingredients of the product manufactured in a piece of equipment, the cleaning aids utilized in the cleaning process and the microbial attributes.