Quality Is a Measurable Process
Quality controls and documentation are defined by product type, formula risk, packaging format, target market and confirmed project scope.
QUALITY ASSURANCE
Quality controls and documentation are defined by product type, formula risk, packaging format, target market and confirmed project scope.
Project-specific quality review, production controls and documentation coordinated according to formula, packaging and target-market requirements.
Routine microbiological limits and applicable pathogen screening are defined by product type and target market. Additional USP/EP-aligned or third-party testing can be coordinated when required.
Accelerated or real-time stability programs can be defined according to formula risk, packaging format and market requirements, with physical, chemical and sensory attributes reviewed at agreed intervals.
In-process checks may include appearance, pH, density and sensory review. Project-specific stability, microbiological, heavy-metal or packaging-migration testing can be coordinated with qualified third-party laboratories when required.
Batch COA and applicable QC records are provided according to the confirmed project scope and release requirements. Supporting third-party reports are coordinated when specified.
Testing parameters are selected according to product type, formula risk, packaging format, target market and the agreed project scope.
pH & Conductivity
Viscosity & Density
Color & Appearance
Odor & Flavor Profile
Active Ingredient Assay
Preservative Efficacy
Heavy Metals Screen
Microbiological Limits