Insights On Pharmaceutical Packaging

1. FAQs On The Revised EU GMP Annex 1: Volume 2 3/5/2025

   Review the implementation of a holistic Contamination Control Strategy (CCS). Discover four key considerations for assessing component readiness: product, process, protection, and proof.

2. Find Flexibility And Scalability With Modular Assembly Equipment 9/30/2025

   Find tailor-made solutions designed to deliver high-quality standards even when scaling up. Modularity enhances production efficiency, saves costs, and shortens time to market.

3. Effective Procurement Strategies For Labeling Systems In Drug Manufacturing 12/11/2024

   What is actually behind the procurement of a pharmaceutical labeling machine and how does the process work? You can find out here what the path to your pharmaceutical labeling machine looks like.

4. A Robust Extractables Data Package Helps Drive Patient Safety 10/1/2024

   Complex drug product formulations are more common, so it is imperative to have a deeper knowledge of extractables to understand risks associated with potential interactions between packaging and product.

5. Collagen Based Products For Regenerative Medicine 1/5/2026

   Sterile packaging is vital for collagen-based regenerative medicine products. Learn how advanced integrity testing methods help prevent contamination, ensuring safety and reliability.

6. Determining The Limit Of Detection In CCIT 12/18/2025

   Accurately determining the smallest detectable defect in pharmaceutical packaging is essential for sterility. Learn how test sensitivity, positive controls, and regulatory standards shape CCI strategies.

7. How DFM Promotes Scalability, Repeatability, And Profitability 6/28/2024

   Find out why it is critical that OEMs see and understand the benefits of taking time to build a mold or create automation more robustly to achieve long-term savings and higher annual production.

8. Ensuring Tablet Logo Legibility: A Critical Step In Preventing Medication Errors 11/11/2024

   Tablet debossing aids medication identification and must meet FDA standards. Font, scale, color, shadow, and stroke details are key for optimal legibility and safety.

9. De-Risking The Transition From Vial To Drug-Device Combination Product 7/25/2025

   When transitioning from a vial to a combination product system, the best approach is to have a holistic de-risk strategy with an intentional focus on the patient, the plan, and the product.

10. The Team For Your Package Design Needs 8/16/2025

    Our dedicated team of in-house design specialists deliver insightful packaging design and practical knowledge to deliver differentiated and cost-effective packaging solutions.