Regulatory Affairs Consulting

Not all companies need full time regulatory affairs staff. In those scenarios, using a regulatory affairs consultant will help your organization keep up with the ever-changing world of regulatory compliance. Nucro-Technics offers Canadian regulatory affairs consulting services for the pharmaceutical, cosmetic, medical device, natural health product (NHP), and biotechnology industries and can help guide you through the complex maze of regulations to help ensure that your products reach, and stay in the market, in an efficient and compliant way with end-to-end support to help you navigate the Canadian market.

What types of regulatory affairs consulting services are offered?

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
  • Cosmetic Label Review
  • Cosmetic Notifications
  • Disclosure of Cosmetic Ingredients Reviews (SOR/2024-63)
  • 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.
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