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Technocraft

Overview:

data processing,data entry, clinical data and reports
i have 5 years of experience in clinical research for new drug development and and's from us and have extensive experience reviewing patient data , regulatory documents, regulatory submissions, final data reviews, i also, have 5 years of software application development experience, i can help you in sdlc documents, iq/pq/oq documentations . compliance's and regulatory submissions.
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  • United StatesHillsborough
  • Oct 2015
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  • United StatesHillsborough
  • Oct 2015
    Member Since