Every vial and ampoule we make carries the same standard behind it. Certified quality systems, regulatory approvals on file, and a manufacturing process built to be repeatable, batch after batch.
First hydrolytic class glass, USP & EP compliant, for maximum chemical inertness. Every vial and ampoule holds its shape and its chemistry from fill to use.
Plants operated to cGMP and ISO 15378, the GMP standard built specifically for pharmaceutical primary packaging, across every factory.
Drug Master Files filed with the USFDA and Health Canada. Every customer receives a Letter of Authorization free of charge and on time.
Every lot carries a unique number, traceable from raw material to dispatch and kept for five years. That number follows the batch through to its certificate of lot clearance.
A greenfield, QbD driven facility with integrated inspection and robotic final assembly, built to catch variation before it ever leaves the plant.
Dedicated mould design and development for custom vial and ampoule specifications, kept in-house so new tooling does not wait on an outside vendor.
A quality record built on QbD, automated inspection and rigorous QA release, backed by a dedicated Quality Team spread across every factory.
Established export logistics delivering on time to pharmaceutical customers across India, Europe, North America, South America, the Middle East, Africa, Russia and Asia Pacific.