Natural Health Product regulatory support, made simple.
Helping Canadian NHP companies prepare compliant documentation, support NPN submissions, and build quality systems that scale with your brand.
- Product Licence Application complete
- Ingredient evidence reviewed
- Label text verified against monograph
- Finished product specifications attached
Compliance work, handled by someone who actually reads the regulations.
Focused, document-first regulatory and quality support tailored to natural health product companies operating in Canada.
NPN Submission Support
Support with Natural Product Licence applications, submission preparation, ingredient information review, and regulatory documentation.
Label Compliance Review
Review product labels for required regulatory elements and help identify compliance gaps before launch.
SOP Development
Creation of clear GMP-aligned SOPs, procedures, and quality documentation for manufacturing operations.
Quality Documentation
Development of batch records, packaging records, forms, logs, trackers, and controlled documents.
A boutique practice for health brands that take compliance seriously.
Regulatory and quality support focused on helping health product businesses navigate compliance requirements efficiently — from your first NPN to a full quality system.
We work alongside founders, formulators, and contract manufacturers to translate Health Canada expectations into documents your team can actually use. No legalese, no copy-paste templates — just clean, defensible documentation.
Not affiliated with Health Canada. We do not guarantee approvals.
Everything we deliver is auditable, versioned, and ready to use.
Four steps from formulation to filing-ready.
Understand your product
Formula, claims, intended market, and timelines. We map the regulatory landscape unique to your product.
Review regulatory requirements
Identify applicable monographs, evidence requirements, and labelling obligations under the NHPR.
Prepare documentation
Draft submission packages, quality records, and SOPs — written for clarity and audit-readiness.
Support compliance readiness
Refine, train, and hand off so your team can maintain compliance long after the engagement ends.
Representative work across the NHP lifecycle.
Sample engagements that illustrate the depth and shape of our regulatory and quality documentation work.
NHP regulatory documentation
Submission-ready packages including PLAs, monograph attestations, and ingredient summaries.
Label compliance review
Bilingual label audits for cautionary statements, claims, and required NHP elements.
GMP documentation systems
Quality manuals, batch records, deviation logs, and CAPA workflows for manufacturing.
SOP creation
Operational SOPs for sampling, testing, cleaning, calibration, and document control.
Tell us about your product.
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