Management systems

Many of our locations are certified according to internationally applicable standards that promote economic, ecological and social sustainability aspects. With clearly defined processes, responsibilities and goals, we contribute to the safety and health of our employees, the responsible use of energy and the careful use of resources.

• DIN EN ISO 9001 – Quality management systems - Requirements
  With our quality control according to DIN EN ISO 9001 ff., we carry out regular material and system tests. The results of these tests form the basis for the further development of our know-how and the constant improvement of the quality of our products.

• IATF 16949 – Quality management system requirements for automotive production and relevant service parts organisations
  With the IATF 16949 as an international standard for the automotive industry, we have implemented quality processes that are specially designed for the requirements of the automotive industry. In this way, we take into account all the requirements that arise in the supply chain in the automotive industry.
   
• DIN EN ISO 13485 – Medical devices - Quality management systems - Requirements for regulatory purposes
  When manufacturing products for medical technology, the focus is on patient and user safety. As a standard for quality management systems in medical technology, DIN EN ISO 13485 describes, among other things, requirements for the development, manufacture, sale and monitoring of the products. Our locations certified according to the standard ensure in their processes that these requirements are systematically complied with, controlled and documented.
   
• ISO 15378 – Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) 
  The production of primary packaging for medicinal products is associated with a high level of responsibility for the quality and cleanliness of our products and thus for the users / patients. Our ISO 15378-certified locations meet the high requirements of the corresponding quality management system and good manufacturing practice (GMP - Good Manufacturing Practice), which are required for primary packaging for medicinal products. In addition to the requirements of ISO 9001, the standard contains detailed specifications for good manufacturing practice (GMP).
   

• DIN EN ISO 14001 – Environmental management systems - Requirements with guidance for use
  ISO 14001 specifies requirements for the environmentally friendly orientation of operational processes. We plan and optimize our processes and procedures systematically according to the requirements of the standard and thus continuously improve the use of resources in our company. This includes, for example, the careful use of resources in the manufacturing process and the avoidance of waste in production and in the office.

• DIN EN ISO 50001 – Energy management systems - Requirements with guidance for use
  DIN ISO 50001 describes the requirements for companies to introduce and implement an energy management system. We systematically record and control our energy flows according to the requirements of the standard. In this way, we regularly determine potential savings and use our resources more sustainably.
   
• DIN ISO 45001 – Occupational health and safety management systems - Requirements with guidance for use
  The health of our employees has the highest priority. The standard facilitates the integration of occupational health and safety in all business processes and creates even better awareness of safety at work at all levels.
   
• ISCC Plus
  ISCC PLUS (International Sustainability & Carbon Certification) is one of the world's leading certification systems for the use of bio-based and recycled raw materials. Our ISCC Plus-certified locations promote the use of sustainable raw materials.

Some certificates are available in our download center:

https://www.roechling.com/de/download-center?data=Zertifizierungen%20ISO