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Clinical Research Administration, High Quality Clinical Research | ISO 1348 | 510K Appr... - 0 views

www.arazygroup.com/ResearchAdministration

clinical research administration high quality ISO 1348 510 approval MDD 93 42 CE markings marking certification FDA medical device regulation

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    The Clinical Research Administrator facilitates the timely execution and completion of high-quality clinical research by assisting investigators and industry sponsors with all aspects of the clinical research.
arazy-group

Medical Device Regulations for Argentina | Argentina Registration Expert - 0 views

arazygroup.com/ice_registration_in_argentina_

Medical Device Registration Consultants Consulting Expert

shared by arazy-group on 25 Jul 11 - No Cached
  • arazy-group on 25 Jul 11
     
    Arazygroup.com - Services in Argentina include in Argentina medical devices are regulated by The National Administration of Drugs, Food and Medical Technology (ANMAT) under the Ministry of Health. Medical products whether they are manufactured or imp.
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