✓ Health Canada DEL • FDA Registered & Inspected • 15+ Years Experience
Sterile Vial Filling —
Exact Dose, Faster to Clinic
Clinical or small-scale commercial batches upto 10,000 vials—filled in a Grade A Pharmaceutical Environment safeguarding and maintaining the highest standards of quality, sterility and compliance.
Why Drug Developers Choose Dalton
Proven expertise, advanced automation, and fully Integrated end-to-end services
Aseptic manufacturing know-how refined across 3000+ campaigns with consistent, reliable results.
Multimodal Suite designed for flexibility, speed and decontamination between production campaigns. Patriot® line upto 30 vials/minute, compliantly.
Strong Inspection Record
Health Canada DEL
FDA Inspected
PMDA and IS0 1345 (2026)
At-a-Glance Capabilities
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Aseptic Simulations Matrix
Saves time and money |
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RABS-Enclosed Fill Line
Upgraded HEPA filtration in Grade A environment |
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Integrated Services
Integrated Solutions for R&D, Process Development, GMP manufacturing, QC testing and Quality Assurance oversight |
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Your Seamless Fill-Finish Journey
From feasibility to CMC filing—streamlined for speed and compliance
Feasibility Call
Outline formulation, batch size and timeline requirements
Tech-Transfer
Risk-based approach minimizes re-validation needs
Grade A Fill-Finish
In-process weight checks, 100% visual inspection
QC/QA Release
Data packages ready for your CMC filing
Talk with our Aseptic Team Today
Our experts are ready to discuss your sterile filling needs.
