Pharma Packaging

The Packaging Design Group knows the pharmaceutical and OTC markets as well as anyone in the packaging distribution business. Our commitment to the pharmaceutical industry is why we only work with qualified manufacturing partners that support the quality and material demands of our clients.  We understand the time-sensitive nature of an FDA submission. PDG will manage the collection of documentation needed for ANDA/NDA submissions to the FDA and continue to support those needs through commercialization.

Documentation Provided:

  1. Product Drawing
  2. Resin Specification
  3. Colorant Specification
  4. Liner Specification
  5. DMF Access Letters
    • Component Vendor L.O.A.
    • Resin Manufacturer’s L.O.A.
    • Colorant Manufacturer’s L.O.A.
    • Liner Manufacturer’s L.O.A.
  6. Certificate of Compliance Sample
  7. Letters, Statements, Assurances from Vendors as needed
  8. USP Test Results as they pertain to USP 661,667
  9. Child Resistance Closure Protocol Results