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Regulatory Affairs - RA, NDS, S/NDS, IND, DIN, NHP

Regulatory Affairs

NUCRO-TECHNICS offers Canadian regulatory affairs and quality assurance for the pharmaceutical, medical device, and biotechnology industries. Among the services that we offer are the following:

  • New Drug Submissions (NDS)
  • Supplemental New Drug Submissions (S/NDS)
  • Investigational New Drug Submissions (IND)
  • Applications for DIN products
  • Medical Device Registrations
  • Applications for Natural Health Products (NPN)
  • GMP Audits
  • Government Liaising and Strategy
  • Validations
  • Regulatory and Quality Assurance Services

NUCRO-TECHNICS‘ clients, ranging from multi-national companies to start-ups, have one attribute in common: An appreciation of the level of expertise and excellence that the NUCRO-TECHNICS team brings to each project.

For further information or to receive a quotation for these services, please contact NUCRO-TECHNICS.