Distribution & Strategic Supply
Reliable, repeatable supply chains for established distributors, procurement teams, and institutional research partners.
The Distribution Program
Built for recurring supply, our distribution program discusses production planning alongside the analytical requirements and quality controls agreed for your project. We build supply agreements around your forecasting and fulfilment needs, subject to feasibility and written scope.
Custom and recurring supply enquiries
- Contract pricing and supply terms scoped per enquiry
- Recurring supply arrangements subject to written scope
- Packaging and labelling options confirmed per agreement
- Production planning discussed as part of scoping
For smaller or one-off requirements, please submit a standard catalog inquiry.
Qualification & Scoping
Establishing a distribution agreement requires a comprehensive alignment of our manufacturing capabilities with your supply chain requirements.
1. Initial Inquiry
Provide your target compounds, expected annual volumes, and desired delivery schedules. Specify if you require finished vials or bulk API.
2. Feasibility & Scoping
Our production team reviews your request to assess raw material availability, analytical requirements, and production planning, subject to feasibility.
3. Contract & Allocation
Where feasible, we set out contract pricing, agreed specifications, production planning, and a recurring supply framework in written terms.
Prepare Your Request
What to Include in Your Inquiry
A complete technical and commercial brief helps us assess feasibility, define the supply framework, and prepare a quotation against the correct specification.
- 01
Product Scope
List catalog compounds or custom sequences and specify whether you require finished lyophilized vials, bulk API, or both.
- 02
Volume Forecast
Provide the initial order quantity, expected annual volume, preferred release quantities, and anticipated ordering frequency.
- 03
Material Specification
Define target purity, salt or counterion form, desired vial fill quantity, and any application-specific acceptance criteria.
- 04
Packaging & Brand
Describe vial, label, and secondary packaging requirements, including any private-label or white-label presentation.
- 05
Analytical Package
Specify the analytical methods and documentation you require — such as HPLC, LC-MS, and a CoA — so the package can be scoped for your internal review.
- 06
Delivery Plan
Share destination countries, requested delivery cadence, temperature-control needs, and documentation required for import review.
Infrastructure & Quality Systems
Volume supply demands consistency. Our manufacturing pipeline integrates analytical verification with logistics capabilities scoped to each supply arrangement.
Analytical Verification
Analytical methods such as reverse-phase HPLC purity data and LC-MS identity confirmation can be included to support documented review across recurring supply, scoped and confirmed per enquiry.
Batch Documentation
A batch Certificate of Analysis covering parameters such as purity, identity, appearance, and net content can be provided to support your receiving and internal review procedures, confirmed per enquiry.
Batch Allocation
Where feasible, planned allocations can be discussed to help partners manage lot continuity and reduce avoidable variation across recurring supply, subject to written scope.
Recurring Deliveries
Manage inventory without holding excess stock. Recurring draw-downs can be structured against a master purchase agreement, with cadence and terms confirmed in writing.
API & Custom Synthesis
Beyond finished catalog vials, we provide bulk active pharmaceutical ingredients alongside sequence-to-vial custom synthesis, with project scale and terms confirmed per enquiry.
Logistics
Shipments can be arranged with tracking, temperature-controlled options where required, and documentation to support customs clearance, confirmed per order.
Secure Your Supply Chain
Partner with a manufacturer that treats your supply continuity as seriously as you do. Begin the qualification process today.