Analytical Test Procedure (ATP) & Certificate of Analysis (COA)

At QPP Enterprise Ltd., we understand that in today’s competitive pharmaceutical, cosmetics, herbal, and food industries, quality and compliance are non-negotiable. That’s why we provide Analytical Test Procedures (ATP) and Certificates of Analysis (COA) for all raw materials, chemicals, and machinery supplied to our clients.

These certifications and testing methods guarantee that the products we deliver meet international quality standards, safety requirements, and regulatory guidelines. By ensuring every shipment is accompanied by valid ATP and COA documents, QPP Enterprise Ltd. builds trust, transparency, and reliability with every client.

What is Analytical Test Procedure (ATP)?

The Analytical Test Procedure (ATP) is a standardized method used to determine the identity, quality, purity, potency, and safety of raw materials and finished products. ATP ensures that every product supplied by QPP is thoroughly tested before reaching the client.

Key aspects of ATP include:

• Chemical Testing – Verifying the composition and purity of raw materials.
• Microbiological Testing – Ensuring no harmful bacteria, fungi, or contaminants are present.
• Physical Testing – Evaluating particle size, solubility, viscosity, and stability.
• Performance Testing – Confirming that the material or machinery performs as expected in the production process.

With ATP, clients receive full transparency and confidence that products are safe and reliable.

What is Certificate of Analysis (COA)?

The Certificate of Analysis (COA) is an official document issued by the supplier or manufacturer, confirming that the product has been tested and complies with specific quality parameters. Each COA includes detailed data on product testing results, proving compliance with industry standards and regulatory requirements.

Typical information in a COA includes:

• Product name and batch/lot number.
• Date of manufacturing and expiry (if applicable).
• Results of chemical, microbiological, and physical tests.
• Compliance statement with pharmacopeia or regulatory guidelines (USP, BP, EP, WHO, etc.).
• Authorized signatures from qualified testing authorities.

A COA serves as proof of authenticity, safety, and regulatory compliance for every product supplied.

Importance of ATP & COA in the Industry

• Pharmaceuticals – Ensures raw materials meet stringent regulatory standards for medicines.
• Cosmetics & Toiletries – Guarantees safe, effective, and allergen-free beauty products.
• Unani & Ayurvedic Products – Confirms purity of herbal ingredients and absence of harmful contaminants.
• Food Industry – Ensures safety, hygiene, and nutritional compliance.
• Machinery & Chemicals – Validates operational efficiency, safety, and consistency.

By maintaining ATP and COA, QPP helps clients meet local and international compliance requirements with ease.

Why Choose QPP Enterprise Ltd. for ATP & COA?

• Trusted Testing Partners – Collaboration with certified laboratories.
• Complete Transparency – Every batch supplied is traceable and backed with documentation.
• Regulatory Compliance – Conformance with WHO, FDA, GMP, ISO, and international pharmacopeias.
• Customer Assurance – Confidence in quality, safety, and performance.
• Continuous Monitoring – Regular updates to meet evolving industry standards.

In Summary

At QPP Enterprise Ltd., Analytical Test Procedure (ATP) and Certificate of Analysis (COA) are more than just paperwork—they are the foundation of trust and quality assurance. By delivering products that are scientifically tested, documented, and certified, we ensure our clients receive nothing less than excellence, safety, and compliance.