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  • ¿QUÉ HACEMOS?
  • INDUSTRIAS
  • PROCESOS
  • CLIENTES
  • EN
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    • ¿QUÉ HACEMOS?
    • INDUSTRIAS
    • PROCESOS
    • CLIENTES
    • EN
COTIZAR
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  • ¿QUÉ HACEMOS?
  • INDUSTRIAS
  • PROCESOS
  • CLIENTES
  • EN
  • …  
    • ¿QUÉ HACEMOS?
    • INDUSTRIAS
    • PROCESOS
    • CLIENTES
    • EN
COTIZAR
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  • INDUSTRIES

    Throughout these 5 years we have focused in the creation of high specialty plastics
    for the pharmaceutical industry, our technology, facilities, professional team and high quality

    standards gives us the capacity to manufacture for different industries like:

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    INJECTION MOULDING

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    INJENCTION
    BLOW MOULDING

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    INJECTION-STRETCH
    BLOW MOULDING

  • PROCESSES

    We manufacture products for high added value industries utilizing autonomous
    manufacturing systems, oil-free high-tech autonomous machinery and high accuracy

    resin and pigment mixers.

     

     

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    EQUIPMENT

    In Inova Pharmaplastics we work with cutting-edge technology in state of the art facilities

    in order to achieve top level standards for pure and high value industries.

     

    • 100% electric machinery
    • Compressed air oil-free ISO-8573

    • Statistical process control (SPC) and 100% in-line verification
    • High level equipment with contactless measuring processes
    • HVAC with terminal HEPA filters (99.99% efficiency)

     

    CLEAN ROOM

     

    ISO-7 and ISO-8 qualified clean room with epoxy finishes.

    • ISO 14644 and USP
    • ISO-7 (10,000 Class number)
    • ISO-8 (100,000 Class number)

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    OUR STANDARS

    In Inova Pharmaplastics we deliver the highest value results for our clients,

    basing our work system in the following standards:

     

    • ISO 9001.

     

    • ISO 15378 Primary packaging materials for medicinal products — Particular requirements
    for the application of ISO 9001:2015, with reference to Good Manufacturing Practice (GMP).

     

    • NOM-059 Good Manufacturing Practices to Drug Manufacturing.

     

    • 21 CFR 820 is a set of regulations from FDA that outlines the current good
    manufacturing practice (CGMP) requirements that medical device manufacturers in the

    United States must follow with regards to their quality system.

     

    • ISO 13485:2016 Medical devices — Quality management systems — Requirements for

    regulatory purposes.

     

    • NOM 241 Good Manufacturing Practices to Medical Devices.

     

    Socially Responsible Company

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    CLIENTS

    Every single one of our clients is as important, reason why we provide personalized
    assistance and the best specialized products. This is how we can create value for

    them and help achieve their goals.

    LABORATORIOS SOPHIA

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    Phone: +52 (33) 2993 2552
  • REQUEST

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