This guidance document applies to all drug submission/application typesFootnote 1including: 1. Clinical Trial Application (CTA), Clinical Trial Application - Amendment (CTA … See more Guidance documents are meant to provide assistance to industry and health care professionals on how to comply with governing statutes and regulations. Guidance documents … See more WebMar 28, 2016 · Activities and Societies: Core Subject Areas: • Pre Market Regulatory Submissions Health Canada- eCTD format CTA, NDS, SNDS, ANDS, NC; NHP licensing applications, Medical Device licensing...
DUPIXENT® (dupilumab injection) now approved by Health Canada for
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