Nucro-Technics offers Canadian regulatory affairs consulting services 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.

Let’s Work Together
For further information about these services, a complete list of services available, to receive a quotation, schedule a test, or if there is something specific that you require, get in touch.