Kushkie Beauty
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Specialized audit for cosmetics factories focused on Good Manufacturing Practices (GMP), hygiene, and quality control systems to ensure product safety and integrity. Our purpose is to globally transform quality processes, ensuring your products are reliable and safe.
Our professional audit service is designed to support cosmetics and personal care manufacturers in achieving compliance with Good Manufacturing Practice (GMP) standards and enhancing their overall quality management systems. This comprehensive evaluation ensures that production processes meet international regulatory requirements, promoting product safety, consistency, and reliability.
Thorough review of manufacturing facilities, procedures, and documentation to align with global GMP guidelines.
In-depth analysis of quality control practices, raw material sourcing, batch traceability, and personnel training.
Helps prepare for audits by authorities such as FDA, EU Cosmetics Regulation (EC) No1223/2009, and other regional standards.
Identifies inefficiencies and provides actionable recommendations to improve operational excellence.
Assists in developing or refining SOPs, batch records, and quality manuals to ensure full traceability and compliance.
Achieve certification required for entry into regulated markets, including North America, Europe, and Asia.
Proactively identify and address potential non-compliance issues before they impact production or reputation.
Receive expert guidance to maintain high standards and adapt to evolving industry regulations.
Strengthen trust with clients, partners, and consumers through verified adherence to global best practices.
What is a Cosmetics GMP and Quality System Audit?
It is a thorough on-site or remote evaluation of a manufacturing facility to ensure compliance with Good Manufacturing Practices (GMP). It verifies hygiene, quality management systems, production workflows, and raw material controls to guarantee product safety and consistency.
Which international standards do your audits prepare us for?
Our audits help align your processes with major global frameworks, including FDA guidelines for cosmetics, the EU Cosmetics Regulation (EC) No 1223/2009, ISO 22716, and other regional market regulations.
How does the Quality System Evaluation minimize manufacturing risks?
By checking batch traceability, raw material sources, contamination risks, and staff training, our audits identify gaps before they escalate. This reduces product contamination risks, recalls, and regulatory violations.
What documentation support is provided?
We assist you in reviewing and optimizing standard operating procedures (SOPs), batch records, and quality manuals to ensure full traceability and complete preparedness for external or government inspections.
How does process optimization improve our manufacturing facility?
The audit helps reveal hidden bottlenecks and redundancies in production workflows. Addressing these allows factories to lower production costs, boost capacity, and improve yield quality.
