Newsletter | November 18, 2024

11.18.24 -- Is Executive Leadership At Today's CDMOs Up To The Job?

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Discover new efficiencies in bioprocessing! Hear from subject matter experts as they uncover how innovative cell line development platforms and enhanced data access help streamline complex biotherapeutic production, from mAbs to ADCs. Presented by KBI Biopharma experts. Watch now.

FEATURED EDITORIAL

Is Executive Leadership At Today's CDMOs Up To The Job?

A report from WittKieffer's Global Life Sciences provides a macro analysis of the executives that helm today’s CDMOs. Competent executive leadership should be a main driver of business-to-business confidence. So as a component of your CDMO due diligence, are you adequately assessing the senior executives at that organization? If so, do they inspire confidence that theirs is a well-governed and operated entity?

Maintaining Harmony With Your CDMO Using 'The Middle Way'

Sponsor and CDMO relationships are fertile ground for conflict. A measured approach can mitigate disruptions with troublesome contractors and high performers alike.

INDUSTRY INSIGHTS

Liposomes – Challenges And Opportunities

Liposome technology is an effective drug delivery tool but still presents difficulties. Learn how developers are meeting these challenges and the opportunities for advancement to maximize liposome usefulness.

How An End-To-End CDMO Simplifies, Speeds Drug Development, Manufacture

Access to technical, process, and regulatory experts under one CDMO roof minimizes logistical and cost-related concerns for biopharmaceutical companies while offering improved control over production.

Considerations In Depth Filter Scale-Up

Explore study findings aiming to assist process development scientists and engineers in understanding the structure of depth filter capsules, identifying key parameters for development, and more.

Developability Assessment Of 3 Therapeutic Antibodies

This poster reviews studies for three monoclonal antibody drug candidates utilizing a panel of small-scale, fast, and predictive tests used to evaluate therapeutic antibodies’ developability.

A Flexible Approach To CMC For Fab And Fc-Fusion Development Programs

Characterizing Fab and Fc-Fusion proteins and developing robust manufacturing processes can help usher them to market and provide new treatment options for diseases that are challenging to treat.

Combining An MVA Technology Platform With Innovative Analytical Methods

See how this process development platform for MVA is impacting vaccine manufacturing and supporting the drug lifecycle from process and analytical development through clinical trials and commercialization.

Partnering For Success In Oncolytic Virus Development

Learn how to navigate decision-making at critical steps and find solutions to key challenges in process development and scale-up to expedite oncolytic virus programs.

Maximizing Yield And Minimizing Risk In Aseptic Filling

Explore the process of how a new fill line was planned for and implemented, while also considering how best to mitigate contamination risks.

Small Is Powerful And Sustained

Advances in sustained-release drug delivery could improve efficiency and consistency in drug release, manifesting real-life advantages for patients in the form of enhanced accessibility and compliance.

How Scale-Up Benefits A Clinical Program To Get Results

A scalable manufacture promises increased process understanding and manufacturing flexibility to deliver a robust, reliable commercial product, and it helps with timely delivery to market.

Process Optimization For mAb Commercial Manufacturing

Strategically optimize your upstream and downstream processes and decrease the timeline from optimization to commercial manufacturing.

Scale Your Vaccine Development With Path-To-PAD

Delve into the details of this straightforward approach to maximize yields early in development, leveraging vaccine expertise, robust platforms, and Vero and Quail cell lines.

SOLUTIONS

Capacity Update July 2024: Large Molecule Development

Gain insights into boosting efficiency, fostering innovation, and how integrated capabilities generate value for innovators.

A Complete Set Of Rapid Methods For Adventitious Agent Detection

Following the latest regulatory guidance, explore a range of methods designed for the fast and sensitive detection of adventitious agents in bulk harvest material.

Combining Scientific Knowledge And Advanced Technology

We specialize in the production of sterile biotechnological products in a manufacturing plant that meets the requirements of GMP.

Capacity Update May 2024: Large Molecule Development

The therapeutic promise of biologicals has fundamentally changed health care. Samsung Biologics is committed to helping drug developers bring these promising new therapeutics to patients.

Process Development

Consider our strong process development capabilities in both microbial and mammalian systems used to provide clients with process development, process optimization, and process troubleshooting.

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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