Packaging
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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.
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CentriPAK BioProcess Container Instructional Video
6/17/2021
This video describes the easy three step process to use the CentriPAK BioProcess Container in your application.
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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.
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Navigating Primary Packaging Challenges, Solutions For Emerging Innovators
12/5/2024
If you are in the process of developing a complex or sensitive injectable drug, learn about containment solutions to mitigate your risks and help you get your drug to the patient faster.
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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.
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Oral Solid Dosage Products: Water Activity And Primary Packaging Selection
7/17/2022
Every individual oral solid dosage (OSD) product has different water activity initially and over time. Learn about USP <922> water activity and primary packaging selection of OSD products.
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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.
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Your Contract Manufacturer Partner
12/14/2020
Discover an integrated solution for pharmaceutical companies that offers a broad range of manufacturing services and capabilities to produce high-quality devices.
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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.
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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.