AA GLOBALUSA
Pharmaceutical blister film packs
Industries

Pharmaceutical Packaging

Manufacturers and generic formulators who need primary packaging, secondary packaging and the active ingredient itself to arrive with documentation their QA can release.

Packaging changes on a registered product are expensive, so the specification has to be right the first time and stable afterwards. Structures are selected against stability data rather than catalogue position, and the source plant does not change without notice.

Second-source qualification is a project, not a purchase. Samples have to arrive early enough to run comparative work, documentation has to match what the first source provided, and the plant has to be available for audit. All three are coordinated from the US side, and DMF status is listed per molecule so filing implications are visible before a sample is requested.

Pharmaceutical blister film packs

What this buyer typically sources

  • Blister films and cold-form alu-alu
  • Lidding foil and barrier laminates
  • Dropper assemblies
  • 400+ APIs with DMF reference where held

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