Insights On Pharmaceutical Packaging

1. Extractables And Leachables: Risk Management And Analytical Solutions 10/11/2023

   Partnering with a CDMO that offers comprehensive and robust E&L studies can help facilitate a smooth product launch by ensuring minimal impact from impurities, all while mitigating risks.

2. 3D Screen Printing: Enabling A New Generation Of Complex Formulations 3/17/2025

   Screen-Printed Innovative Drug Technology can produce oral, transdermal, and implantable dosage forms while ensuring heterogeneous distribution of active ingredients.

3. Effective Procurement Strategies For Labeling Systems In Drug Manufacturing 12/11/2024

   What is actually behind the procurement of a pharmaceutical labeling machine and how does the process work? You can find out here what the path to your pharmaceutical labeling machine looks like.

4. Choosing The Right Primary Container And Troubleshooting Issues 8/25/2023

   Selecting the right primary container for an injectable drug product is critical. Discover how to identify relevant testing to de-risk your product development – and quickly uncover causes of failures.

5. The Importance Of Containment In Oral Solid Dose Packaging Systems 8/1/2024

   Containment is growing in importance due to increasingly stringent legal requirements for packaging solid medicines. Learn in detail about containment solutions for the pharmaceutical industry.

6. 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.

7. Achieving EU GMP Annex 1 Compliance For Contamination Control 3/4/2025

   Gain insight into three areas that have been key in ensuring a robust contamination control strategy to help ensure compliance with the updated Annex 1 regulation: planning, people, and products.

8. Design Verification Testing Of Combination Products 7/12/2024

   Developing a combination product and seeking a list of tests to complete design verification testing? Review the details for planning, design inputs, design outputs, and design verification.

9. 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.

10. Innovation For Subcutaneous Delivery Of Large-Volume Complex Biologics 5/9/2024

    Explore the key findings of a new wearable injector clinical trial, including its positive impact on patient experience and the broader benefits of wearable injectors for chronic disease management.