Insights On Pharmaceutical Packaging

  1. Inline Checkweighing Of Packaged Products In Manufacturing 12/29/2025

    Accurate inline checkweighing is vital for quality control. Learn how system design, software, and regulatory compliance work together to overcome high-speed production challenges.

  2. Beyond Visual Inspection: Understanding Acoustical Transparency As A PAT 12/29/2025

    Airborne ultrasound enables non-destructive seal monitoring, detecting subtle material variations. See how this proactive approach enhances consistency, reduces risk, and ensures packaging integrity.

  3. 5 Critical PUPSIT Considerations For Sponsors Targeting The EU Market 1/22/2026

    To ensure compliance with EU GMP Annex 1 guidelines and drug product approval, familiarize yourself with PUPSIT: how it works, why it’s needed, and strategies to maximize success.

  4. Key Considerations When Choosing A Device For Dry Powder Nasal Delivery 10/21/2024

    Building on previous discussions, here we discuss the benefits of nasal delivery and the challenges of developing dry powder formulations by focusing on key devices that can be used for delivering dry powder nasal dosage forms.

  5. Planning For Scale-Up 5/21/2026

    From rapid early-stage production to scalable commercialization, discover the packaging and continuity challenges companies face as they prepare for launch.

  6. Ensuring Integrity: A Comprehensive Approach To CCI 1/8/2026

    Deterministic CCI testing ensures compliance in packaging. Learn how advanced methods like Vacuum Decay, HVLD, and Helium Leak Detection deliver results aligned with USP 1207 and global standards.

  7. Setup Made Simple With The BioTitan Retention Device 5/27/2025

    Find out how quick and simple it is to set up an assembly secured with the Thermo Scientific BioTitan Retention Device.

  8. Solving The Challenges Of Transdermal Patch Package Integrity 1/5/2026

    Ensuring transdermal patch packaging integrity is critical for safety and efficacy. See how advanced methods deliver precise, reliable leak detection, outperforming traditional approaches.

  9. Considerations For Handling A Drug Product With Ultra-Low Temperature Requirements 9/3/2026

    Maintaining product integrity at ultra-low temperatures is complex. Learn key packaging, validation, and supply chain considerations for advanced therapies.

  10. 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.