Newsletter | April 8, 2025

04.08.25 -- Embracing Turnkey And Outsourced Quality Management In Biopharma

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The debate rages on. While the automation that enables continuous processing gets a lot of hype, there are plenty of dyed-in-the-wool biopharma pros who contend that process optimization and intensification yield comparable benefits, without requiring the capital-intensive process overhaul that continuous demands. Join Bioprocess Online Live for a virtual deep dive into the scalability, sustainability, and capital implications of the continuous-versus-optimized debate. Registration is free thanks to the support of Cytiva.

FOCUS ON OUTSOURCING

Embracing Turnkey And Outsourced Quality Management In Biopharma

In-house quality management systems often struggle to keep pace. Many organizations are adopting turnkey and outsourced quality management solutions to ensure compliance and enhance efficiency.

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.

Tech Transfer: 8 Typical Stumbling Blocks To Avoid

Optimize your biopharmaceutical technology transfer by prioritizing clear communication, thorough training, and strategic planning to ensure success.

Address Current Challenges In Gene Therapy Viral Vector Manufacturing

Learn about key advancements at each step in viral vector production  — from maximizing titer output at scale upstream to optimized formulation compositions at fill/finish — to support commercial scale.

How Real-Time Data Access Enhances Collaboration With Your CDMO

Quality data for informed decision-making is well supported by a built-in network of lab digitization solutions and a commitment to the principles of data integrity.

Enabling Subcutaneous Delivery For Improved Patient Compliance

The ability to administer high doses of biologics subcutaneously offers numerous benefits, including reduced treatment burden, patient convenience, and increased adherence to treatment regimens.

Cis-Targeted Immunotherapies Need Large CDMO Expertise And Flexibility

Asher Biotherapeutics was seeking a CDMO that could handle Phase 2 through to commercial production, as well as taking early-stage projects in its pipeline all the way through their lifecycle.

OUTSOURCING SOLUTIONS

Druggability - Mycenax

Consulting Services For Track And Trace Technologies - Koerber Pharma

Capacity Update January 2025: Large Molecule Development - Mabion

Putting The Customer Experience At The Forefront - INCOG BioPharma Services

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