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Drug Packaging Material Properties
May 27, 2017

 Pharmaceutical Packaging Material The packaging materials used in the manufacture of packaging containers, packaging and decoration, packaging and printing, packaging and transportation to meet the requirements of the packaging materials used, it includes metal, plastic, glass, ceramics, paper, bamboo, wild Mushrooms, natural fibers, chemical fiber, composite materials and other major packaging materials, including coatings, adhesives, strapping, decoration, printing materials and other auxiliary materials

  Material properties

  1, a certain mechanical properties

  Packaging materials should be able to effectively protect the product. So should have a certain strength, toughness and flexibility to adapt to the pressure, the impact. Vibration and other static and dynamic factors.

  2, separated performance

  According to the different requirements of the product packaging, packaging materials to deal with moisture, water vapor, gas, light, aroma, odor, heat, etc. have a certain barrier

  3, good safety performance

  Pharmaceutical Packaging Material Packaging materials itself, the toxicity is small, so as not to contaminate the product and affect human health; packaging materials should be non-corrosive, and has pest control, moth, anti-rat, inhibit microbial and other properties to protect the product safety.

  4, the appropriate processing performance

  Packaging materials should be suitable for processing, easy to make a variety of packaging containers should be easy to packaging operations mechanization, automation, to adapt to large-scale industrial production should be suitable for printing, easy to print packaging logo.

  5, the better economic performance

  Packaging materials should be a wide range of sources, easy to draw, low cost, after use of packaging materials and packaging containers should be easy to handle, do not pollute the environment, so as to avoid pollution

  main duty

  1, the development and revision of materials, intermediate products and finished product internal control standards and inspection procedures, the development of sampling and sample system;

  2, the development of testing equipment, equipment, reagents, test solution, standard (or reference substance), titration solution, culture and other management methods;

  3, determine the use of materials and intermediate products;

  4, audit the finished product before the release of production records, decided to issue products;

  5, the audit of nonconforming product processing procedures;

  6, the materials, intermediate products and finished products for sampling, testing, leaving samples, and issued a test report, batch inspection records saved to the product after sales year;

  7, monitoring the clean room (area) the number of dust and microbial number;

  8, the evaluation of raw materials, intermediate products and finished product quality stability, in order to determine the material storage period, the product life to provide data;

  9, the development of quality management and inspection staff responsibilities