Pharmaceutical Packaging Solutions

  1. Jones Packaging And Medication Dispensing Solutions 2/5/2021

    Jones Healthcare Group enables advances in healthcare with packaging components and services that protect product integrity and help consumers make informed decisions. For over a century, our partnerships, knowledge and expertise across healthcare sectors have  uniquely positioned us to respond to evolving market needs with insights and opportunities that help our customers put consumer wellness first.

  2. Used Thermo Scientific VersaRx Checkweigher 7/7/2020

    Used Thermo Scientific Checkweigher, model Versa RX, 304 stainless steel construction, with pneumatic reject, touchscreen HMI, approx. 2,200 hours of use, with 6" wide infeed/outfeed conveyor, 115 volt, serial# A626, built 2014.

  3. Jones Blister Packaging Services 1/31/2021

    Our fully integrated two-lane Uhlmann blister line is capable of multi-product blisters and multi-product cartons, with an entire range of forming and lidding films including PVC, Alu+Alu, and child-resistant formats. Enhanced by a serialization solution compliant to the Drug Supply Chain Security Act (DSCSA), our technology ensures the highest quality and productivity with maximum flexibility.

  4. Used Klockner Blister Packaging System 10/16/2019

    Used Klockner medipak blister packaging unit, Model EAS.

  5. Pharmaceutical Contract Packaging And Filling Services - Tablets, Capsules, Powders 6/5/2019

    With ample available capacity, Ropack Pharma Solutions provides the efficiency of five bottling lines with quick changeovers, online validated fill accuracy and the flexibility to accommodate small lots to commercial runs for the bottling of tablets, capsules and powders.

  6. Feasibility Studies For Container Closure Integrity Testing Applications 7/9/2020

    PTI Inspection Systems are scientific instruments being deployed for high risk packaging applications. The environments in which these systems operate is often highly regulated with test results having a significant impact on operational decisions. The reliability and sensitivity of a CCI test method is critical to assure that correct decisions are made to maintain product quality and patient safety. If PTI’s equipment is going to test your packaging, we aim to deliver the most effective solution. Feasibility studies offer a detailed glimpse into the technological capabilities ahead of critical purchasing decisions. Feasibility studies can also act as a preliminary test method for an application. The results from feasibility or method development testing can be rolled out to the production environment for rapid validation and deployment.

  7. AST Container Closing System 12/27/2019

    AST’s Container Closing System (CCS) is a benchtop, semi-automatic machine that provides complete and accurate control of the syringe and cartridge closing process. The Container Closing System is able to close syringes or cartridges using both vacuum and vent-tube methods for a wide range of container sizes quickly and easily with only a few format part changes.

  8. Test Method Development For Package Integrity Testing 7/9/2020

    A variety of test methods exist to challenge package quality and performance. The objective of a feasibility study is to evaluate if a recommended CCI solution works and establish the optimal test parameters and Limit of Detection (LoD).

  9. Secondary Contract Packaging 12/9/2020

    Leave your packaging details to the experts at Jones
    We offer a wide range of flexible and custom secondary packaging services, including recovery packaging and kitting. Whether you require us to assist with package design and material specifications, provide a finished product including the packaging materials, or assemble your provided components, our facility and processes are equipped to ensure speed to market. Our secondary packaging services are provided by a dedicated Packaging Services business unit.

  10. Clinical Trial Manufacturing And Packaging 7/31/2020

    PCI provides a comprehensive service at each stage of the product lifecycle for a wide range of dosage forms, in full compliance with GMP regulatory standards for both highly potent and non-potent drug products.