Insights On Pharmaceutical Packaging

  1. Evaluating The Entire Package System Under USP 382 5/18/2026

    USP 382 introduces holistic packaging evaluation, focusing on container closure integrity, functionality, and real-world conditions to ensure sterility, safety, and product reliability.

  2. 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.

  3. Choosing The Right Pharma CMO: The 3 Cs That Matter Most 2/27/2026

    Choosing a CMO is a strategic decision that shapes long‑term quality and scalability. Discover how a focused framework helps teams identify partners that can adapt and support growing portfolios.

  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. Ensure Quality Control With Innovative Software 7/1/2025

    Ensure unmatched product quality with an X-ray system paired with an innovative software that detects contaminants and missing items in stacked packaged goods with precision.

  6. Nebulizers: Package Integrity Testing Challenges And Solutions 1/5/2026

    Maintaining sterile packaging for nebulizer drugs is vital to prevent contamination. Learn how regulatory standards and advanced leak detection methods address integrity challenges in high-risk formats.

  7. Optimal Syringe Carton Design To Meet Drug Manufacturers' Needs 8/1/2024

    Learn about the advantages of an optimal packaging design and the resulting benefits of its implementation to the overall process.

  8. Providing Packing And Blinding Solutions For An Innovative Drug Start-Up 9/13/2024

    Discover how a CDMO with integrated services enabled a botanical drug start-up to commence its Phase 1 clinical trial, paving the way for further advancement of its innovative botanical drug.

  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. Secondary Packaging: Inspection, Brite Stock Bottle Labeling, And Cartoning 6/23/2026

    Gain insight into a coordinated, around-the-clock approach that demonstrates how packaging efficiency can keep pace with urgent pharmaceutical launches and tight commercialization timelines.