Quality Control & Testing laboratory
ISO 22716 & ISO 22000 HACCP Certified
B2B Analytical Laboratory

Quality Control & Testing

Comprehensive laboratory testing, microbial bioburden screening, and ICH-compliant stability protocols to guarantee safety and global compliance for your private label products.

Explore Manufacturing
Quality Control & Testing Overview
Analytical & Compliance Summary
AKTO delivers ISO 22716 (GMP) and ISO 22000 certified Quality Control & Testing services for cosmetics, personal care, and dietary supplements. Our analytical suite encompasses raw material verification (IQC), in-process monitoring (IPQC), finished product assay release (FPQC), microbiological safety risk assessment, and ICH-compliant stability and shelf-life testing.

Specialized Quality Control Divisions

Explore targeted testing services across key manufacturing stage gates.

Incoming Quality Control

Detailed technical protocols, equipment specs, and release criteria.

In-Process Quality Control

Detailed technical protocols, equipment specs, and release criteria.

Finished Product Quality Control

Detailed technical protocols, equipment specs, and release criteria.

Stability & Compatibility Testing

Detailed technical protocols, equipment specs, and release criteria.

Comprehensive Quality Control & Testing Services for B2B Manufacturing

At AKTO sp. z o.o., our Quality Control & Testing infrastructure operates under rigorous ISO 22716 (Cosmetics GMP) and ISO 22000 (HACCP) certified management systems to guarantee product safety, structural stability, and full international compliance. We integrate advanced analytical methodologies into every stage of new product development and commercial scaling, serving as an authoritative partner for private label beauty, health, and supplement brands operating across EU, UK, US, Canada, and GCC markets.

Multi-Tiered Analytical Testing Capabilities

Our state-of-the-art laboratory facility delivers end-to-end analytical verification tailored to complex chemical and microbiological profiles across all stage gates of production:

  • Incoming Quality Control (IQC): Raw material identity, purity, and active constituent assays utilizing UV-Visible Spectrophotometry, HPLC, and Gas Chromatography (GC-MS/GC-FID) to verify batch consistency prior to formulation integration.
  • In-Process Quality Control (IPQC): Real-time monitoring of rheological behavior, emulsion stability, pH boundaries, density, viscosity, and organoleptic parameters during batch synthesis.
  • Finished Product Quality Control (FPQC): Comprehensive release testing, active substance quantification, impurity profiling, heavy metal detection, and packaging compatibility verification.
  • Microbiological & Hygiene Safety: Quantitative bioburden testing, pathogen challenge testing, and environmental monitoring guided by expert microbiological risk assessments.
  • Stability & Shelf-Life Substantiation: Real-time, accelerated, and stress stability protocol execution under ICH guidelines to determine shelf-life, packaging barrier performance, and active degradation pathways.

Integrated Quality Assurance & Regulatory Alignment

We seamlessly bridge physical laboratory controls with global market compliance packages. Every testing plan supports technical dossiers including Product Information Files (PIF/CPSR under EU Regulation (EC) No 1223/2009), UK SCPN notifications, Canada CNF/NPN licensing support, and Saudi SASO/SABER certification. Our testing protocols feed directly into your brand's regulatory documentation, ensuring complete audit readiness across international regulatory bodies.

Scientific Advisory & Technical Governance

Our quality assurance and analytical method validation frameworks are directed by leading academic and industrial researchers, ensuring that every product formula design and manufacturing service meets stringent international standards.

See also: Private Label Manufacturing | Formulation & R&D | Regulatory & Documentation | Packaging & Labeling | Logistics & Fulfillment

Frequently Asked Questions

Technical & procedural insights regarding analytical testing and GMP compliance.

AKTO provides comprehensive quality control testing across the full product lifecycle, including incoming raw material identity and purity testing, in-process parameter checks, finished product release testing, microbiological bioburden screening, and accelerated stability and shelf-life substantiation for cosmetics and food supplements.

All new formula design and R&D related activities undergo rigorous physicochemical compatibility testing, challenge testing, organoleptic monitoring, and real-time/accelerated stability testing under controlled temperature and humidity conditions to establish formula integrity and expiry dates.

Yes, AKTO operates under ISO 22716:2007 (Cosmetics GMP) and ISO 22000:2018 (Food Safety Management Systems) standards. Our testing methodology adheres to ICH Q2 principles and relevant pharmacopoeial frameworks for analytical method validation.

Contact our technical team to schedule an initial consultation. We will evaluate your product specifications, raw material requirements, and target markets to build a custom testing protocol and provide a detailed quote.