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  • rapid metal protocasting
  • trolley medical devices
  • trolley medical devices
  • Taroni Foundry specialized in aluminium casting for medical devices participates at EU Gateway │Business Avenues

    EU Gateway │Business Avenues is an initiative funded by the European Union helping European companies to establish long-lasting business collaborations in Asia.

    Selected European companies meeting the eligibility criteria get the opportunity to participate in a one-week business mission focused on a specific sector in Korea, South East Asia, China and Japan. Companies benefit from a range of business support services, which include coaching, logistical, and financial support.

    The Healthcare & Medical Technologies Sector covers a broad range of technologies, products, equipment and devises. Recent trends underline the principles of Circular Economy – reducing material inputs and resource intensity, greater durability or reusability of healthcare and medical devices.
    Relevant sub-sectors include:

    • Assistive technologies: Homecare and rehabilitation equipment, to assist elderly people or people with reduced functionalities. Devices and prosthetics to assist or train elderly people or people with reduced functionalities.
    • Medical equipment: Any instrument, apparatus, device or material used in diagnosing, treating and/or preventing of human or animal diseases, thereby excluding the use of pharmacological, immunological or metabolic means.
    • ICT for health: New or improved equipment might be used for enhancing healthcare, such as miniaturised and cheaper electronics and sensors, high-density memory, micro-electromechanical systems, and novel combinations of existing devices.
    • Telemedicine and remote health monitoring: Homecare, telecommunication networks, radiographs, pathology freeze frames. Examination, observation and treatment of patients and the training of personnel by utilising telecommunications.
    • Nanotechnology healthcare
    • Life Science/ Biotechnology for health: Any technological application that uses biological systems, living organisms or derivatives thereof, to make or modify products or processes for specific use in healthcare; recombinant DNA, cell fusion, and new bioprocessing techniques to produce large molecules useful in treating and preventing disease.
    • Dental products: Diagnostic technologies, Preventive technologies, Oral hard tissue disease treatment technologies, Regenerative medical technologies, Dental laboratory technologies

    www.eu-gateway.eu

  • rapid metal protocasting
  • x ray trolly medical devices
  • x ray trolly medical devices
  • x ray trolly medical devices
  • ISO 13485 Medical device

    Quality Management Systems are an essential requirement for Medical Device Manufacturers and provide evidence of ongoing product quality and regulatory compliance.

    What is the ISO 13485 standard? 

    ISO 13485 is the internationally recognized standard for quality management systems in the medical device industry.
    It specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices, and that related services consistently meet customer requirements and applicable regulatory requirements. It is designed and intended for use by organizations for the design and development, production, installation, servicing and sales of medical devices.  

    The primary objective of ISO 13485 is to facilitate harmonized medical device regulatory requirements for quality management systems. ISO 13485 is a standalone standard. It is largely based on the structure of ISO 9001, but includes some particular requirements for medical devices such as risk analysis, sterile manufacturing and traceability. Organizations certified to ISO 13485 can not claim conformity to ISO 9001

    In 2017 Taroni foundry has obtained the certification of compliance with ISO 13485 on Quality Management Systems for Medical Device.

    DOWNLOAD CERTIFICATE ISO 13485

    Connection with national requirements for approval of medical devices 

    Legal access to markets for products is essential for manufacturers of medical devices. ISO 13485 is often required by national regulations as part of the approval process for medical devices, e.g. for the EU directive on medical devices (Medical Device Directive 93/42/EEC, In Vitro Diagnostic Directive 98/79/EC, Active Implantable Medical Devices 90/385/EEC). 

  • ISO 13485 Medical device

    Quality Management Systems are an essential requirement for Medical Device Manufacturers and provide evidence of ongoing product quality and regulatory compliance.

    What is the ISO 13485 standard? 

    ISO 13485 is the internationally recognized standard for quality management systems in the medical device industry.
    It specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices, and that related services consistently meet customer requirements and applicable regulatory requirements. It is designed and intended for use by organizations for the design and development, production, installation, servicing and sales of medical devices.  

    The primary objective of ISO 13485 is to facilitate harmonized medical device regulatory requirements for quality management systems. ISO 13485 is a standalone standard. It is largely based on the structure of ISO 9001, but includes some particular requirements for medical devices such as risk analysis, sterile manufacturing and traceability. Organizations certified to ISO 13485 can not claim conformity to ISO 9001

    In 2017 Taroni foundry has obtained the certification of compliance with ISO 13485 on Quality Management Systems for Medical Device.

    DOWNLOAD CERTIFICATE ISO 13485

    Connection with national requirements for approval of medical devices 

    Legal access to markets for products is essential for manufacturers of medical devices. ISO 13485 is often required by national regulations as part of the approval process for medical devices, e.g. for the EU directive on medical devices (Medical Device Directive 93/42/EEC, In Vitro Diagnostic Directive 98/79/EC, Active Implantable Medical Devices 90/385/EEC). 

  • Fonderia Taroni sarà presente come espositore a COMPAMED- MEDICA 2018- Düsseldorf, la fiera della subfornitura in ambito medicale dal 12 al 15 Novembre 2018
    Vieni a trovarci allo Stand 8A S32

    Per informazioni ulteriori vista:
    www.compamed.de
    www.medica.de

     

  • Fonderia Taroni will be present as exhibitor at COMPAMED / MEDICA 2018- Düsseldorf, the branch of the medical subcontracting from 12 to 15 November 2018
    Come and visit us at Stand 8A S32

    For more information visit: 

    www.compamed.de
    www.medica.de

     

  • Fonderia Taroni will be present as exhibitor at COMPAMED / MEDICA 2018- Düsseldorf, the branch of the medical subcontracting from 12 to 15 November 2018
    Come and visit us at Stand 8A S32

    For more information visit: 

    www.compamed.de
    www.medica.de

     

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