02.17.26 -- Solving The Top 3 Pharma Packaging/Manufacturing Issues

A thorough and adaptable analytical strategy is essential for navigating the complex mAb market. This approach boosts the likelihood of market approval and unlocks the full potential of these therapies.

Here, we conduct a comprehensive analysis of diverse PROTAC (Proteolysis Targeting Chimeras) structures, evaluating their calculated physicochemical properties to identify key trends.

Learn in detail about High Voltage Leak Detection (HVLD), packaging applications that can be inspected with HVLD, and how to determine the best leak-testing method for your application.

Watch to gain insight into the crucial role of maintenance in ensuring the ongoing optimal performance, reliability, and longevity of your inspection systems.

Ensure cleanroom air quality with optical particle counters. Explore how OPCs work, their performance metrics, and key considerations for choosing the right one.

Bowie-Dick testing ensures steam sterilizers remove air and achieve full steam penetration. Discover why this simple check is vital for compliance, safety, and preventing costly sterilization failures.

Adopted by leading chemical and pharmaceutical firms, MTP-based ACPP aligns with industry standards, offering portable, easily integrated solutions for continuous, efficient API production needs.

Proper planning for first-in-human studies is crucial to successful drug development, which requires innovative trial designs and sound CMC strategies to mitigate risk and expedite proof-of-concept.

Delve into the complexities of scaling decisions to gain insights from biopharma developers and a CDMO, as well as their mutual interest in achieving successful strategies for avoiding common pitfalls.

Find out how pharmaceutical manufacturers are using digital tools to achieve the “golden batch”—a production run that balances quality, efficiency, and compliance through smarter processes.

Even with automation, manual visual inspection remains vital in sterile drug manufacturing. Examine six advanced considerations for refining your operations, ensuring compliance, and minimizing costs.

Technological developments have led to growth in the suitability of fermentation. Observe the impact of the evolution of synthetic biology and supporting technologies on modern fermentation practice.

See how AI is transforming visual inspection and gain a deep understanding of defect detection, real-time performance, and integration challenges.

Read why organizations must integrate data and processes to enhance quality and insights to improve operational efficiency, patient health, and regulatory compliance.

Uncover how continuous processing cuts waste, improves efficiency, and supports safer, scalable reactions while helping teams meet sustainability goals and speed development.

Pharma manufacturing embraces cutting-edge automation, yet outdated paper-based documentation hinders efficiency and delays batch releases. Reveal how digital solutions can transform compliance.

A pharmaceutical company facing storage space issues decided to outsource its reference samples to Q1 Scientific, a stability storage service provider, resulting in cost savings.