Regulatory Open Forum

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  • 1.  Adverse Events Training

    Posted 28-Sep-2015 08:15

    I am looking for a webinar or seminar on Adverse Event training.  I've been scheduled for two over the past year and they were cancelled due to lack of attendance. Thanks.

     

    Donna Smith

    Sr. Regulatory Affairs Project Manager

    Description: Description: <a href=image002.gif@01C9AC6F.D25DA6B0">

    38505 IH 10 West

    Boerne, Texas  78006

    Office: 210-581-0720

    Fax: 210-581-1413

    Email: donna.smith@missionpharmacal.com

    www.missionpharmacal.com

     



  • 2.  RE: Adverse Events Training

    Posted 28-Sep-2015 09:12
    Donna,

    This is for your consideration.

    LIVE | Implementing Global Medical Device Adverse Event Reporting Systems in EU, Canada and US |Tri-monthly | 11: 00 AM PST | 02:00 PM EST | 60 Minutes | Register Here

    LIVE | Implementing Medical Device Complaint Handling Systems | Bi-monthly, 2nd Thursdays | 01:00 PM PST | 04:00 PM EST | Duration: 60 Minutes | Register Here

    Recorded | Complaint Handling and Medical Device Reporting (MDR) | 62 Minutes | Read More Here. 


    Thank you.  

    s/ David
    ____________________________________________________________
    Dr. David Lim, Ph.D., RAC, ASQ-CQA 
    President and CEO | REGULATORY DOCTOR and GCS
    Phone (Toll-Free): 1-(800) 321-8567


    "Knowledge is power only when it is practiced and put into action." - Regulatory Doctor

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