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Regulatory Affairs Internships

Regulatory affairs internships โ€” FDA, CDSCO, EPA submission workflows, dossier preparation, and product-approval lifecycle exposure.

What is a Regulatory Affairs Internship?

This internship gives you visibility into how regulated products โ€” drugs, devices, agrochemicals, biologicals โ€” actually reach the market. You shadow the dossier compilation, submission, and follow-up processes that bridge R&D and regulators.

What you will do

  • Study real regulatory submission templates โ€” CTD, e-CTD, ANDA, NDA, IND
  • Map product approval pathways across CDSCO, FDA, EMA, EPA where applicable
  • Prepare and review module sections of representative dossiers
  • Track regulatory queries (deficiency letters) and response workflows
  • Maintain regulatory archives to industry-grade documentation standards

What you take away

  • NTHRYS internship certificate with regulatory-scope detail
  • Hands-on familiarity with the dossier formats employers actually use
  • Understanding of submission timelines, queries, and approval-tracking
  • A targeted CV credential for regulatory affairs careers

Pick the field below to see specific regulatory affairs project options.

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