Sterile kits
Area-based procedure kit
Area-based kit that brings mops, wipes and task accessories into one procedure set.
Sector directory
Pharmaceutical manufacturing
Particles, microbial risk and chemical conditions.
Define your needsScope
Which acceptance criteria are defined for the task and zone?
Pre-selection is not site validation.
Environmental class
Classification of airborne particle cleanliness.
Sterility
Scope of the validated process and packaging.
Product performance
Findings obtained with a specific sample, method and conditions.
In this category
Cleanroom wipes
Cleanroom wipe
Wipe for cleanroom surfaces, assessed for dry use or wet use with a chemical.
Absorbent pads
Spill control pad
Absorbent pad for liquid and chemical spill control, with single-use and reusable options.
Entry and particle control (planned)
Entry and transfer area textile (planned)
Planned product line for particle control in entry and transfer areas, to be assessed in a site pilot.
Mop systems
OWMO BIO single-use mop
Single-use mop for short tasks, assessed in 2, 3, 4 and 5-layer constructions.
Autoclave systems
OWMO ECO autoclave system
Mop head and wipe system designed for reuse after laundering, packing and steam sterilisation.
Mop systems
OWMO ECO reusable mop
Mop reused after controlled laundering, assessed in 2, 3, 4 and 5-layer constructions.
Evidence dossier structure
- Method
- Which question is being addressed, using which method.
- Sample
- Identity of the product and configuration under review.
- Condition
- The environment and parameters of the test.
- Revision
- Document version and applicable scope.
No report is currently approved for publication.
Technical dossier consultation
Read a result with its sample.
When method, sample or test conditions change, the scope of results is reassessed.
Review the evidence dossier structureLet's start with your process conditions.
Assess environment, surface, chemistry and use cycle together.