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
- 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.