Canadian Pharmaceutical Consulting You Can Trust
Androxa provides pharmaceutical CRO/CMO consulting, Health Canada compliance, NHPD licensing, and GMP advisory services for the Canadian life sciences industry.
Our Services
Pharmaceutical CRO/CMO Consulting
Strategic guidance for contract research and manufacturing organizations navigating Canadian regulations.
Health Canada & NHPD Licensing
End-to-end support for Natural Health Product notifications, Drug Identification Numbers, and regulatory submissions.
GMP Compliance & Auditing
Gap assessments, remediation plans, and audit preparation aligned with Health Canada GMP requirements.
Regulatory Training & Workshops
Hands-on GMP, NHPD, and Health Canada compliance training for pharmaceutical teams.
About Androxa
Androxa is a Canadian pharmaceutical consulting firm specializing in CRO/CMO advisory, Health Canada regulatory compliance, NHPD licensing, and GMP readiness. We help life sciences companies navigate the Canadian regulatory landscape with confidence and precision.
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Frequently Asked Questions
Q1. What services does Androxa provide?
Androxa specializes in pharmaceutical CRO/CMO consulting, Health Canada regulatory compliance, NHPD licensing support, and GMP audit preparation. We guide companies through every stage of the Canadian regulatory process.
Q2. Who does Androxa work with?
We work with pharmaceutical companies, natural health product manufacturers, contract research organizations (CROs), contract manufacturing organizations (CMOs), and startups entering the Canadian market.
Q3. What is NHPD licensing and do I need it?
The Natural and Non-prescription Health Products Directorate (NHPD) requires a Natural Product Number (NPN) before selling natural health products in Canada. Androxa handles the full application process including product classification, evidence compilation, and submission.
Q4. How long does a Health Canada submission take?
Timelines vary by submission type. NPN applications typically take 30–120 days for review. Drug submissions can take longer. Androxa helps you prepare complete, first-pass-ready dossiers to minimize delays.
Q5. Can Androxa help with GMP compliance?
Yes. We perform GMP gap assessments, develop remediation plans, create standard operating procedures (SOPs), and prepare your team for Health Canada inspections.
Q6. Do you provide training services?
We offer hands-on workshops covering Health Canada GMP requirements, NHPD regulatory pathways, quality system documentation, and audit readiness for pharmaceutical teams.
Q7. Can I schedule a consultation?
Absolutely. We encourage prospective clients to book a consultation to discuss regulatory goals, compliance gaps, and project timelines.
Q8. Where is Androxa based?
Androxa serves Canadian pharmaceutical and health product companies from coast to coast. Contact us at [email protected] for consultations.