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.