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  • 1.  CFDA, PMDA, ANVISA & IMDRF newsletter subscription

    Posted 16-Feb-2018 04:27
    Edited by Francesco Taddeo 16-Feb-2018 04:32
    ​​Hi,

    Does anyone know how to subscribe to the medical device guidance newsletter for China (CFDA), Japan (PMDA), Brazil (ANVISA) and IMDRF?

    Thanks a lot in advance.

    Kind Regards,

    Francesco Taddeo

    ------------------------------
    Francesco Taddeo
    Innsbruck
    Austria
    ------------------------------
    ​​


  • 2.  RE: CFDA, PMDA, ANVISA & IMDRF newsletter subscription

    Posted 18-Feb-2018 12:08
    Hi, Francesco,

    The RAPS Regulatory Focus has medical device news and pharma on a daily and weekly basis.  I would say start there.

    Emergo has an excellent website for world news.  The link below takes you to their world news home page.  From there you can look up news by market area.  You can also sign up for their newsletter.

    Global Medical Device Consulting
    Emergo remove preview
    Global Medical Device Consulting
    Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.
    View this on Emergo >

    Regards,

    ------------------------------
    John Minier, RAC
    Consultant, Principal
    john@johnminier.com
    (914) 850-4432
    Highland Mills, NY
    United States
    ------------------------------

    Original Message


  • 3.  RE: CFDA, PMDA, ANVISA & IMDRF newsletter subscription

    Posted 19-Feb-2018 09:31
    ​Hi John,

    Thanks for the information provided and your helpfulness.

    Kind Regards,

    Francesco

    ------------------------------
    Francesco Taddeo
    Innsbruck
    Austria
    ------------------------------

    Original Message


  • 4.  RE: CFDA, PMDA, ANVISA & IMDRF newsletter subscription

    Posted 20-Feb-2018 09:12

    China Med Device LLC publishes weekly as well as monthly CFDA News Roundup.  It covers the latest China policies, regulations, QA/recall/AE, and new approvals in medical device and IVD etc. It is exciting times as CFDA is expected to go through major structure changes with more standards and guidelines for the complete product life cycle in 2018, and we at China Med Device, LLC are the thought leaders and experts to guide you through this change. You can find under our resources and blogs for CFDA information and Opt-in our newsletters. We help western companies with their entire regulatory product life cycle with our proven methodology. visit China Medical Device - Accelerate Your Device's Entry Into China

    China Med Device remove preview
    China Medical Device - Accelerate Your Device's Entry Into China
    China Med Device - specialize in accelerating Western medtech companies with turn-key solutions for China FDA regulatory&CRO services and commercialization.
    View this on China Med Device >

     



    ------------------------------
    Grace Fu Palma
    China Med Device, LLC
    MA, U.S.
    gpalma@chinameddevice.com
    978-390-4453
    www.chinameddevice.com
    ------------------------------

    Original Message


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