Newsletter | April 15, 2024

04.15.24 -- Getting To Know MAM, The New Quality Control Strategy On The Block

SPONSOR

Four Steps To Identifying The CDMO Proposal Worth Signing

Transparency and communication are essential to the success of a manufacturing partnership. If a CDMO is unwilling to have frank conversations during the proposal phase, that’s likely a red flag. The right partner’s team will help you make educated choices while ensuring quality, reasonable costs, and timeline efficiency.

FEATURED EDITORIAL

Getting To Know MAM, The New Quality Control Strategy On The Block

When characterizing PQAs, the multi-attribute method offers a one-stop shop for analysis. This article explores technical considerations for this emerging strategy.

INDUSTRY INSIGHTS

Dynamic Trends Shaping The Future Of Microbial Fermentation

Drug developers must understand the latest trends in microbial fermentation. By leveraging innovative methods and technologies, developers can unlock new opportunities and improve patient outcomes.

Bacteria Media Optimization Using In Silico Strategies

Determining ideal media composition for a bacteria is critical because it fosters a satisfactory grow rate, allowing the bacteria to reach the required growth yield.

Importance Of Assessing Mannitol Crystallinity In Lyophilized Drug Products

Drug product stability may be seriously compromised if mannitol completes crystallization during storage rather than during the freezing step in the lyophilization process.

Imaging Large Volume Subcutaneous Injections To Inform Clinical Design

New higher volume, higher viscosity pharmaceutical formulations for subcutaneous injection, alternatives to traditional intravenous treatment, enable chronic disease therapy in alternate settings.

Early Development To Clinic – De-Risking A Bioconjugate’s Journey

The journey of a novel bioconjugate into clinic is complex and uncertain. Explore the challenges of moving a bioconjugate candidate from early development into clinic.

Quality Implications Of CO2 Sensing In Bioreactor Applications

Review the technologies underpinning sensors utilized in dissolved CO2 measurement devices and determine which sensors are appropriate for your application.

SPONSOR

Webinar: Unlocking the potential of your Sterile Injectables with exact SI-ence 

The pathway from early clinical phases to commercial is not straightforward, particularly for complex sterile injectable products. It is important to have a wide range of specialized capabilities to keep pace with the rapidly evolving market. Global Pfizer experts will explore key aspects of the sterile injectable journey, including factors to consider during the development and tech transfer stages. Click here to learn more.

SOLUTIONS

Capacity Update February 2024

As we expand our mammalian capacity across the manufacturing network, updates on completion dates and capacity availability are presented in the session.

Antibody Drug Conjugates: Link Your Antibody To Its Fullest Potential

Learn how our parallel development service works seamlessly with our existing antibody capabilities, helping to accelerate your ADC program and reach market faster.

SUREmAb - Monoclonal Antibody Development, The Way It's Meant To Be

Leverage robust development strategies and enable an optimized process for mAb development and manufacturing, efficiency and speed with exceptional quality, and high titers with lower-cost workflows for maximum ROI.

OUTSOURCED PHARMA CAPACITY UPDATE

Find Your New CDMO At Outsourced Pharma Capacity Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capacities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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