Meishida Pharmaceutical Packaging Quality Control

As a specialized pharmaceutical packaging manufacturer, our packaging quality control system not only complies with international standards, but also ensures that every batch of product meets the stringent requirements of the pharmaceutical industry.

Quality Control Processes for Pharmaceutical Packaging

We use state-of-the-art technology and equipment, combined with our experienced team, to provide our customers with high-quality, compliant packaging solutions.

1. Raw Material Inspection

We select raw materials that meet international standards, including plastics, paper and other materials that meet FDA and ISO22000 certification requirements. All suppliers are rigorously audited to ensure the quality and safety of the materials.

2. Production Process Monitoring

Our production lines are equipped with automated testing equipment to ensure that every step of the process meets design requirements. Real-time monitoring identifies potential quality issues and makes immediate adjustments.

3. Sample Inspection

Dimensions, print quality and material uniformity are checked to ensure that packaging at each stage of production meets the required quality standards.

4. Finished Product Inspection

Each batch of pharmaceutical packaging undergoes a rigorous finished product inspection to ensure dimensions, appearance, sealing, durability and compliance with food and pharmaceutical grade safety standards.

5. Inspection Reports and Certifications

We provide comprehensive inspection reports for each batch of products produced to ensure that they meet the requirements of international certifications such as FDA, SGS and ISO.

6. Final Inspection and Packaging

Upon completion of production, our quality control team conducts a final inspection of all finished products to ensure product integrity and compliance with all quality standards before packing.

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Professional laboratory and excellent instrument testing

Meishida strictly follows ISO9001:2015 quality management system to execute systematic management. Through the whole process control from incoming materials, semi-finished products, finished products to shipping inspection, we ensure that each batch of products complies with international regulations and quality standards, and provide accurate and reliable test results.

Advanced Class 10,000 Professional Laboratory

Our company has a GMP-compliant 400m2 class 10,000 standard laboratory with advanced testing equipment to provide a strict testing environment for the quality of pharmaceutical packaging.
The laboratory covers the testing of materials, semi-finished products and finished products such as laminated films, bags and cartons, and strictly monitors the production and inspection environment to ensure that each product meets the highest standards in the industry.

Explore Our Pharmaceutical Packaging

First-class Testing Instruments

The laboratory is equipped with advanced precision testing instruments to fully support all quality tests and ensure that all products meet the highest safety and performance requirements.

Gas Chromatograph: for detection of solvent residues or volatile organic compounds (VOCs) in packaging materials to ensure material safety.

Water Vapor & Gas Transmission Rate Tester: Used to determine the sealing of packaging materials and effectively block external substances to maintain the quality of pharmaceuticals.

Electronic Tensile Strength Tester: It is used to test the peeling strength and heat sealing strength to ensure that the pharmaceutical products are not damaged during transportation and storage.

Friction Coefficient Tester: It is used to test the coefficient of friction of packaging materials and evaluate the sliding and adhesion between materials, especially in the automated packaging process.

Fourier Transform Infrared (FTIR) Spectrometer: Used to identify materials and ensure that packaging materials comply with the quality standards of the pharmaceutical industry, avoiding the use of substandard or harmful raw materials.

Dust Particle Counters: Used to detect the number of dust particles in the packaging production environment to ensure a dust-free environment. Ensure that pharmaceutical packaging is not contaminated.

Bio-safety Cabinet and Ultra Clean Bench: Used for sampling microorganisms in a sterile environment to ensure that the packaging process is not contaminated by microorganisms and to guarantee the safety of pharmaceuticals.