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Clinical Trial Supplies

Tri-Pac team can assist in expediting product development through production of clinical trial materials. Our lab, innovation and compounding scientists and engineers work directly with your team to assist with technology transfers for clinical trial supplies, registration batches and commercial launches. 


We have extensive experience in handling and cGMP manufacturing of aerosols, liquids, tubes, lotions, and other dosage formats. 


Services include

  • Study protocol

  • Statement of BSE/ TSE Compliance

  • Stability Study (Shelf life)

  • Quality/ Technical Agreement

  • Supplier Qualification

  • Batch Records

  • Artwork reproduction

  • API Methods for Raw/ Finished Goods

  • Cleaning Validation

  • Production Validation

  • Method Development/ Validation

  • Ethics Approval

  • Others

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