Supplemental New Drug Submission (SNDS), Health Canada eCTD
Build supplements in the product's existing eCTD lifecycle and validate every sequence before you file. For sponsors filing in-house and consultancies filing for clients.
SNDS Filing Workflow
See where supplements lose time across drafting, review, validation, and readiness.
Write the Canadian Module 1 for Each SNDS Sequence
Assyro writes ca-regional.xml to Health Canada's Module 1 schema 2.2 with the SNDS regulatory activity type.
Stop Schema Errors Before the Build
A Module 1 that does not match the Canadian schema is stopped before the sequence is built.
Validate Against Health Canada's Rules
Each sequence is checked against Health Canada's eCTD validation rules, version 5.3.
Keep the Lifecycle in Order
Each sequence records the sequence it relates to, so the dossier's history stays readable.
SNDS Filing Controls and Capacity
Keep submission growth controlled with clearer ownership, better traceability, and consistent execution across active programs.
Maintain Audit-Ready SNDS Records
Supplement sequences are checked against Health Canada's Module 1 schema 2.2 and eCTD validation rules version 5.3, with audit trails and role-based access.
Manage More SNDS Programs With the Same Team Size
Track Health Canada correspondence and commitments in Assyro RIM
Guides for your next decision
Explore requirements, compare workflows, and prepare your evaluation.
Questions About SNDS Submission Software
Practical questions sponsors and consultancies ask about Health Canada supplements.
