How it works
Our process is transparent and built for Regulatory Affairs and R&D teams. From request to delivery in five steps; development and study-driven timelines.
Share Your Requirements
Start by sharing your molecule list, target SRA market, and study requirements. You can upload a file, enter details manually, or search our database of 1000+ products.
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Upload your molecule list (Excel, CSV, or PDF)
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Specify target SRA market (FDA, EMA, MHRA, etc.)
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Indicate study type and timeline requirements
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Note any temperature or storage requirements
We Confirm Availability
Our team reviews your request and confirms RLD availability from our network of SRA-origin suppliers. We verify batch details, expiry dates, and realistic lead times.
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Product availability confirmation
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Batch numbers and expiry date options
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Accurate lead time estimates
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Alternative options for hard-to-source items
Receive Your Quotation
Within 24-48 hours, you'll receive a detailed quotation with transparent pricing, sourcing origin details, and a comprehensive documentation summary.
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Transparent pricing with no hidden fees
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Sourcing origin and market details
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Documentation checklist included
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Shipping and logistics options
Approve & Procure
Once you approve the quotation and shipping conditions, we initiate procurement. You'll receive regular updates on order status throughout the process.
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Simple approval process
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Secure payment processing
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Real-time order status updates
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Dedicated account manager support
Receive Your Product
Your RLDs arrive with complete shipment records, temperature logs (if applicable), and all documentation needed for your regulatory submission.
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GDP-compliant packaging and handling
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Temperature logs for cold chain products
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Complete chain of custody documentation
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Documentation typically required for regulatory submission
Typical Timeline
From request to delivery, here's what to expect
Submit your requirements via our portal or email
Receive detailed quotation with availability confirmation
Order processing, sourcing, and quality verification
GDP-compliant shipping to your facility
What You Receive With Every Order
SRA-origin reference products
Products from FDA, EMA, MHRA, and other stringent regulatory authority markets; batch and expiry visibility provided.
Complete Documentation
Certificate of Analysis, batch records, and all paperwork needed for regulatory submission.
Temperature Records
Continuous temperature logging and excursion reports for cold chain products.
GDP-aligned handling
Documentation demonstrating handling aligned with labeled storage and common industry practice throughout the supply chain.
Traceability Records
Complete chain of custody from origin market to your facility door.
Dedicated Support
Account manager support for questions, issues, or future procurement needs.
Ready to get started?
Submit your requirements and receive a quotation within 24-48 hours.