Insights On Pharmaceutical Packaging

  1. Selecting Container Closure Systems With Confidence: Lyophilization 3/7/2024

    Experts take you through the entire selection process for primary packaging components for lyophilization and provide aspects to consider for all relevant attributes.

  2. Why A Leading Manufacturing Partner Chose NeoTOP Packaging Machines 8/2/2024

    Learn how a leading CDMO partnered with Körber to quickly deploy a high-speed packaging solution to meet tight production deadlines in the face of a global pandemic.

  3. CDMO Installs Toploading Packaging Solutions To Meet Small Lot Needs 7/30/2024

    Gain insight into the solutions a global leader in contract packaging and clinical supply services relies on to address clients' evolving needs for the small lot packaging of specialized and personalized drugs.

  4. Designing Robust Studies To Meet Auto-Injector Performance Requirements 10/30/2025

    Learn more about the critical tests for ensuring the proper performance of auto-injectors, which are used for a variety of applications ranging from emergency use to treating chronic conditions.

  5. A Practical Packaging Components Checklist For Emerging Biotechs 6/20/2024

    A proactive approach to packaging development can ultimately ensure a smoother launch. Explore five key considerations when selecting components for your injectable drug product.

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

    The revised GMP Annex 1 guidelines emphasize quality risk management, enhanced environmental monitoring, and data integrity, which aim to minimize contamination and ensure patient safety.

  7. 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.

  8. New Standards For Elastomeric Components In Sterile Packaging 1/20/2026

    USP’s new elastomeric packaging standards shift testing to full system‑level evaluation, strengthen integrity and usability expectations, and place compliance responsibility on drug developers.

  9. Bridging The Gap Between Product Readiness And Equipment Availability 12/15/2025

    Discover how manual precision at scale bridges packaging gaps, accelerates product launches, and ensures uninterrupted supply to deliver quality when automated equipment isn’t yet operational.

  10. FT-IR Identifies Contaminants And Helps Avoid Hazards And Product Loss 3/7/2024

    Fourier Transform Infrared Spectroscopy (FT-IR) is a reliable method with multiple applications when it comes to identifying both intrinsic and extrinsic compounds in a drug product.