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Quality & environment
Depending on the packaging specifications, BRODART PACKAGING relies on the most suitable plant of the group: standards, certification etc.
Quality
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Plant of Tilwel
Plant of Brodart
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Plant of Breger Centre
In order to meet the expectations and market requirements, the BRODART INDUSTRIES Group is committed to a comprehensive approach to providing a safe, quality , made in an environment where risks are identified and controled.

We attach great importance to the concept of quality. In this context, every step of our production is subject to strict control.

In addition, all components of the product are identified allowing full traceability .

Our quality control laboratories perform tests and specific analyzes throughout product manufacture. More broadly, quality control laboratories of BRODART PACKAGING work closely with professional associations, raw materials suppliers, packaging machinery manufacturers.
They all contribute to adapt the packaging in accordance with the recent French and European standards.
Environment
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Plant of La Halle
Plant of Tilwel
Involved for a long time on the environment, our sites have developed a proactive policy in this area by:  

  • Eco-design by reducing the source of raw material (less weight, less thickness ...)
  • Recyclable packaging design.
  • Treatment of solvents.
  • Treatment of all waste by selective courses (cardboard boxes, office paper, polyethylene, polypropylene, polyester).
Hygiene
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Plant of Breger Centre
Plant of Brodart
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Plant of Tilwel
The implementation of a risk analysis process, the application of hygiene rules in the production plants and storage facilities, strict monitoring or existing regulations, help to ensure food security of the product delivered to the customer.
Safety of pharmaceutical packagings
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Plant of Tilwel
Our specialized plant TILWEL BRODART PACKAGING is organized to meet the requirements of the ISO 15378 standard on the safety of pharmaceutical packaging:  

  • Ensuring patient safety in view of the risk of contamination.   
  • Ensure that packaging materials are in compliance with the legal requirements of the pharmaceutical industry on medicines.
  • Ensuring that recognized GMP rules are followed and that the standard management system is effective and efficient.