Avoid Regulatory Risk with Marshall Plastic Film, a Quality Systems Leader

10/21/15

If you aren’t aware of the interactions that can occur between your products and the intermediate bulk packaging that they are stored in, your company could be at regulatory risk. In the pharmaceutical industry, improper storage – or storage in unsuitable containers – can result in the degradation and contamination of products.

At Marshall Plastic Film, our plastic bag liners and pharmaceutical bags are designed to eliminate these risks and ensure the integrity of your products. Our highly educated staff is trained to adopt a health care mentality and provide solutions to highly complex pharmaceutical concerns. Additionally, our engineers can tailor those solutions to meet your specific product requirements.

Utilizing state-of-the-art equipment that allows us to test the FT-IR, DSC, seal, burst and tensile strengths of our polyethylene films and bags, we’re able to provide our clients with an unmatched level of consistency and product repeatability. Furthermore, our in-house testing lab, utilizing our OPTO process control system, ensures that the quality that you need is the quality that you receive.

By monitoring and controlling all extrusion film processes, we are able to exercise a high level of control over the manufacturing process. As each lot is produced using the same extrusion line and the same set points as the previous lot, we are able to guarantee that lots are consistent and offer the same high level of quality.

At Marshall Plastic Film, we want our clients to feel comfortable with the knowledge that their intermediate bulk packaging will prevent degradation and contamination. As a leading provider of packaging bags for pharmaceutical companies, we take our commitment to quality seriously. If you’ve been searching for an ideal supplier of polypropylene bags for the pharmaceutical industry, contact the staff at Marshall Plastic Film today to learn more about what we have to offer.

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