Packaging

1. Key Considerations When Developing Your Combination Product 2/20/2024

   Succeed in combination product development by understanding the risk factors that may arise and implementing mitigation strategies that will streamline the device development process.

2. Human Factors Testing: Engaging End-Users In Med Device Development 3/11/2025

   Explore the significance of human factors in the development of medical devices through an illustration of how important it is to incorporate the end users in the device development process.

3. CentriPAK BioProcess Container For Cell Culture Separations 6/17/2021

   This video highlights the Thermo Scientific CentriPAK BioProcess Container. This next generation centrifuge container provides a single-use, sterilized, closed system for cell culture separations.

4. Managing Risks In Injectable Drug Delivery 3/13/2025

   Gain insights pertinent to efficient and effective drug development. Understand and execute a risked-based critical thinking approach related to injectable drug packaging and delivery.

5. Selecting Container Closure Components: Extractables And Leachables

   Primary packaging components require a thorough assessment to ensure safety and efficacy. Plan ahead and start your assessment early to mitigate your risks, delays, and out-of-pocket costs.

6. Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs 1/13/2025

   Check out this exciting video showcasing the key advantages of Alba®: innovative coating technology that reduces potential interaction between the drug and container surface.

7. New Guidelines For Container Closure Integrity Testing 12/20/2018

   Increased regulatory scrutiny and exciting new analytical technologies have altered the landscape of container closure integrity testing. In order to provide guidance to this new environment the US Pharmacopoeia revised Chapter <1207> Sterile Product Package Integrity.  View this webinar recording to learn about the new guidelines and how they will impact your approach to sterile product package integrity.

8. A Science-Based Approach For Ensuring Container Closure Integrity Of Sterile Vials 3/15/2021

   Recent regulatory guidance has triggered changes in industry best practices in the area of container closure integrity (CCI) testing. A more science-based holistic approach that includes robust design & qualification of the process and the implementation of appropriate process controls is required. This webinar will describe a framework to enable such a holistic approach to CCI that assures both the primary packaging and the process contribute to good CCI of sterile injectable vial product.

9. The Enhanced Version Of Ready-To-Use Vial Platform 1/13/2025

   Discover a platform for aseptic manufacturing that offers pre-sterilized vials for biologics to improve efficiency and safety with automated filling systems and advanced packaging for optimized drug containment.

10. How To Optimize Labeling In A Pharmaceutical Environment 5/29/2025

    Accurate, readable pharmaceutical labels are crucial. Learn to navigate considerations like printing, application tolerances, and inspection to select the right machinery for your production environment.