Professional pharmaceutical consulting and unlimited CTD template requests from our 20-year CDMO team. Get regulatory documentation support and strategic guidance in 48 hours.
Direct access to our formulation scientists and regulatory experts. Book instantly, get guidance within 48 hours.
60-minute video consultation for rapid guidance on your development challenges.
Comprehensive 2-week engagement with detailed formulation and manufacturing analysis.
Custom project-based engagement for complete dossier preparation and submission support.
Get custom regulatory templates for any molecule, delivered in 48 hours. Plus monthly intelligence reports and priority support.
Unlimited template requests • 48-hour delivery • Priority support
Any CTD module (1-5), any molecule, any dosage form. Non-confidential starter templates customized with your drug name. Request via email to subscription@burrardpharma.com
FDA/EMA/Health Canada updates, biosimilar opportunities, patent cliff alerts, and regulatory pathway changes affecting your pipeline
20% discount on all advisory services, 24-hour email response guarantee, and direct line to our formulation team
20% off PureMonograph.ai for automated drug monograph research and CTD compliance checking (Code: BURRARD20)
Simply email your request to subscription@burrardpharma.com
We'll deliver customized non-confidential templates via email within 48 business hours.
A complete regulatory documentation ecosystem for your development pipeline.
Use PureMonograph.ai to search 61+ databases, get drug monographs, and automated compliance checking
Subscribe to Burrard Intelligence and request custom regulatory templates for your specific drug product
Book advisory calls for strategic guidance, gap analysis, and regulatory pathway planning
Transfer technology to Burrard CDMO for GMP manufacturing and regulatory submission