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Regulatory Affairs Intern

Internship Hanoi, Vietnam
Health & Biotech
Health & Biotech
10 July 2024
  • Tracking legal documents, submissions regularly. Update registration license if any.
  • Ensure all submissions, both planned and on-going, are logged and tracked regularly.
  • Support RA executive to review product labels and package inserts of registered pharmaceutical products as well as medical devices.
  • Archive and maintain regulatory files in a format consistent with local health authority and corporate requirements: such as photocopy, scan,
  • Support documents related submission required for tender…as per requested.
  • Perform other administrative works and necessary activities related to regulatory affairs upon RA Manager request.
  • Support other admin work of Baxter office if any.

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