Product Qualities

We providing the high-quality products and services at every stage is non-negotiable because It’s what earns us trust and respect and we would’t have it any other way.

Quality assurance is essential in ensuring that products meet the required standards. Our quality management system is implemented and maintained by trained staff to meet the requirements set forth in ISO/IEC 17025 and ISO 17034. This quality management system is applicable to all activities associated with the manufacture and testing of certified reference materials in ISO-accredited laboratories. It involves consistent checks and monitoring throughout the production process. This helps identify and fix any issues before products reach customers, ensuring their satisfaction and trust.
Quality Assurance in Research Chemicals Peptides Cytokines Proteins Recombinant Enzymes etc
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Delivering Safe and Effective Solutions
We sell pure research chemical substances
Quality is built into everything we do, from our people to our processes, products and services. We believe that investing in quality leads to profitability through competitive pricing, regulatory community trust, an empowered workforce, and improved turnaround time.
Quality and Certifications
We are committed to ensuring and maintaining the highest degree of quality and reliability in all aspects of our reference material production.

Each Reference Material (RM) and Certified Reference Material (CRM) is goes with documentation complying with ISO standards testing laboratories and RM producers. Analytical Standards are go along with a standardized product information.


We include;

- Certificate of Analysis (CofA) that reports the certified concentration and corrected purity values,

- Certificate of Analysis (CofA) that reports identity, purity, and other relevant characteristics, displaying a minimum of two purity and two identity characterization tests.

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Working with ISO/IEC 17025:2017 Accreditation partners

Our Quality Approach

We have invested in promoting a culture of exceptional quality. Our quality assurance department represents 10% of our workforce, and they offer guidance and oversight at every stage of a product’s development and manufacture.

Our business model and Quality Systems are designed to achieve consistent product quality through thoughtful quality planning, control and measurement. Pii’s Quality Systems consist of four key elements: process performance and product quality monitoring, corrective action and preventive action (CAPA), change management, and internal, customer and regulatory inspections. This data is compiled, analyzed and regularly reviewed as part of Pii’s Key Performance Indicator (KPI) program. This continuous improvement philosophy ensures that we meet and exceed current GMP requirements.
ISO/IEC 17025:2017
Working with ISO/IEC 17025:2017 promotes confidence that the laboratory is meeting the general requirements for the competence of testing and calibration thereby demonstrates the ability to generate valid results necessary for reliable characterization of RMs and CRMs.