Notice: Submission Filing Requirements - Good Manufacturing Practices (GMP)/Drug Establishment Licences (DEL)

Evidence of Good Manufacturing Practices (GMP) for drug submissions. The goal of this revision is to better align the drug submission screening and review process with the Drug Establishment Licence (DEL) process. This should allow sponsors to make timely drug submissions while still providing adequate assurance of an establishment’s commitment to quality.

Publisher
Health Canada
Resources
2
Catalogue metadata updated
2021-07-08

Data overview

Formats
HTML
File languages
English, French

Official sources and licences

Resources

Related open data