Our Approach
Specification-first
Product families are engineered to meet real SOPs in Pharma/Biotech, Medical Devices, Semiconductor, and Optics/Diagnostics.
Process control
Defined parameters for every critical step—edge sealing, laundering, saturation, drying, and packaging.
Traceability
Each lot carries its own history, from raw materials to final inspection and labeling.
Clean Manufacturing Environment
Our production lines operate in controlled areas with defined gowning, air handling, and housekeeping routines.
- Classified clean zones with HEPA-filtered airflow and positive pressure differentials.
- DI water management for washing/rinsing where applicable.
- Clean packaging (e.g., double-/triple-bagging on specified lines) to preserve product integrity to point-of-use.
Outcome: Lower particulate burden from converting through final pack-out.
Laundering, Drying & Surface Cleanliness
Where required by the product design, we use controlled washing and rinsing to reduce residues.
- DI water rinses and defined drying cycles for surface cleanliness.
- Filtered airflow drying with monitored time/temperature windows.
- Contact controls to avoid re-contamination during transfer and bagging.
Outcome: Tight control of NVR and particle levels for sensitive applications.
Pre-Wetted (Presaturated) Technology
Reliable solvent loading improves repeatability at the bench.
- Standard systems: IPA/DI water blends at defined percentages (others available by request).
- Saturation control: Target weight windows verified inline; sealed packaging to retain loading.
- Label clarity: Solvent ratio, saturation weight, and safety information printed on pack.
Outcome: Fewer variables during wipe-downs and equipment prep.
Sterile Processing (Where Applicable)
For sterile variants, we partner with validated sterilization providers.
- Validated sterilization routes (e.g., gamma, EtO as applicable to the SKU).
- Lot-specific certificates available upon request.
- Handling protocols to protect sterile barrier integrity through shipment.
Outcome: Sterile options aligned to aseptic workflows. (See product page for method and availability.)
Testing & Validation
We support qualification with documented test methods and typical values (see TDS).
- Particles (e.g., ≥0.5 μm)
- Non-Volatile Residue (NVR) in DI and IPA
- Ions (e.g., Na/K/Cl) where relevant
- Absorbency / wicking, tensile/abrasion
- ESD characteristics for designated SKUs
Documentation you can request
- TDS (Technical Data Sheet) · SDS (Safety Data Sheet) · COA/COC · Sterility certificate
Outcome: Faster audits, clear comparisons, and smoother approvals.
Quality System & Traceability
- Incoming inspection of substrates and packaging components.
- In-process checks at converting, laundering, saturation, and pack-out.
- Lot coding and record retention for each shipment.
- Nonconformance & CAPA workflows that feed continuous improvement.
Outcome: Lot-to-lot consistency and clear accountability.
Environmental Responsibility
We build durability and cleanliness into products while managing resource use.
- Efficient converting to reduce offcuts; targeted recycling where feasible.
- Smart packaging protection without excess.
- Chemical stewardship and worker safety practices across lines.
Outcome: Products that meet performance needs with sensible material choices.
Continuous Improvement & R&D
- Pilot runs to trial new fibers, edge profiles, and saturants.
- Joint development with customers for niche processes.
- Statistical monitoring of critical parameters to reduce variation over time.
Outcome: A roadmap of incremental gains—cleaner, stronger, and more predictable materials.
Technology Highlights (At-a-Glance)
- Sealed-edge converting (laser/ultrasonic)
- DI rinse & controlled drying (where applicable)
- Presaturation lines with inline weight checks
- Classified pack-out & clean packaging
- Validated sterilization paths for sterile SKUs
- Lot-level documentation and quick COA/Sterility requests