Capabilities · Quality Assurance
Checked at every gate. And documented.
Every production stage checked, tested, and documented, from intake to Certificate of Analysis.
ISO 9001:2015
Certified quality management
6
QA stages per batch
6-9 Months
Sample retention period
15+
QC parameters tested per batch
As an ISO 9001:2015 certified organization, Asiatek maintains a comprehensive quality management system that governs every stage of manufacturing. Our Quality Control Station combines rigorous testing technology with skilled professionals carrying out inspection at each critical control point. Incoming materials are tested and approved before they enter production. Key process parameters are monitored in-process. Finished batches are tested against specification in our Quality Control Laboratory before release.
“Quality assurance at Asiatek is structured in six stages. A batch can be stopped at any one of them.”
Behind the testing sits the record. Every batch ships with a Certificate of Analysis, and a dedicated QA room retains samples from every incoming and outgoing batch for six to nine months, so if a question ever arises about a product in the field, the answer comes from a retained sample and its batch record, not from recollection.
The Quality Control Laboratory: the final checkpoint before any batch is cleared for release.
Quality assurance
Six stages. One standard.
Incoming Inspection
Every raw material verified against specification before release to production.
In-Process Inspection
Key process parameters monitored live at each critical control point during blending and filling.
Batch Testing
Finished batches tested against specification: physical, chemical and performance properties.
Laboratory Validation
Formal QC Lab sign-off before any batch is cleared for release.
Batch-to-Batch Consistency
Retained samples checked against prior batches for ongoing consistency.
Documentation & CoA
Certificate of Analysis and full batch records issued with every shipment.
Incoming Inspection
Every raw material verified against specification before release to production.
In-Process Inspection
Key process parameters monitored live at each critical control point during blending and filling.
Batch Testing
Finished batches tested against specification: physical, chemical and performance properties.
Laboratory Validation
Formal QC Lab sign-off before any batch is cleared for release.
Batch-to-Batch Consistency
Retained samples checked against prior batches for ongoing consistency.
Documentation & CoA
Certificate of Analysis and full batch records issued with every shipment.
Batch testing
Fifteen parameters. Every batch.
“Tested against specification” is a specific claim. These are the parameters a batch is measured on before the Quality Control Lab clears it for release.
Viscosity
pH Level
Density & Specific Gravity
Flash Point
Appearance & Colour
Odour
Corrosion Resistance
Moisture Content
Active Ingredient Concentration
Foam Test
Freeze-Thaw Stability
Packaging Integrity & Leak Test
Spray Pattern Consistency
Particle Size Distribution
Internal Pressure
Leak testing station, aerosol line
Water bath testing station, aerosol line
Quality & compliance
The standards that matter to procurement teams.
International Standards
ISO 9001:2015 certification governs our quality management system, the same standard that OEM and enterprise procurement teams require from tier-one suppliers globally.
Regulatory Compliance
Formulations, labelling and safety data documentation are prepared to meet the regulatory requirements of target markets, including export destinations where requirements differ from domestic standards.
Global Export Readiness
Quality systems and documentation are built for international supply chains: batch records, CoA formats and compliance documentation structured for cross-border procurement teams.
Multi-Level QA
Release authority sits with the lab, not the line. Production teams run the checks at their stations, but only a formal QC Lab sign-off clears a batch for dispatch; quality is an independent function, not a self-assessment.
Documentation & Traceability
Full traceability from incoming raw material lot to outgoing finished batch. Retained samples at both ends of the process mean questions can be answered accurately, not approximately.
Safe & Reliable Formulations
Safety data is documented for every formulation: material compatibility, toxicity profile, handling requirements. Safe chemistry isn't assumed; it's verified and on file.
Quality you can audit.
Our facility is open to inspection. We provide full documentation on request.