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  • 1.  Resources to learn hands-on regulatory requirements and documentation

    Posted 29-Nov-2023 23:21
    Hello Community! 
    I am interested in hands-on learning on US FDA regulatory requirements for Medical devices. There are several resources (including RAPS) which outline regulations. However, I am searching for resources/courses which provide hands-on learning, example documentation, assignments etc. so that I can gain practical knowledge. 

    If anyone knows such a resource/course focused on the EU and other regions, those are also appreciated. 


    Thanks!


  • 2.  RE: Resources to learn hands-on regulatory requirements and documentation

    Posted 29-Nov-2023 23:58
    Dear All, 
    WE do offer a course on  FDA Medical Devices Regulations.
    Please reach out to ne  at guparmg1952@gmail.om

    Perfection is our Passion and Pride
    Wishing you a good day

    Rajkumar Gupta
    (M. Pharm)

    Director- Perfect Pharmaceutical Consultants Pvt. Ltd
    CTD/eCTD/ US DMF/CEP/ANDA/ WHO GMP/Open & Close Part DMF 
    Prestige Classic (D Wing)
    Dawa Bazaar, Pune Mumbai Express Highway,
    Chinchwad, Pune 411019, Maharashtra, India.
    Mobile:9371020504
    To know more about is visit  www.perfectdossier.com
    Place inquiry/order at  guptarmg1952@gmail.com


    NO DMF./ NO GMP =  LESS  BUSINESS
    FILE DMF/COMPLY GMP =  MULTIPLY     BUSINESS



    Original Message


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