Newsletter | July 9, 2024

07.09.24 -- Selecting A Manufacturing Partner

SPONSOR

A ballooning clinical-stage ADC development community is putting stress on both manufacturing capacity and antibody engineering and conjugation talent. What does this burgeon mean for ADC manufacturing, process development, and, ultimately, clinical progress? Join Bioprocess Online Live on July 9th as we navigate the complexity of the ADC manufacturing environment. From linkers to payloads to conjugation, we’ll cover the lay of the land for developers. Registration is free thanks to the support of Cytiva.

FOCUS ON OUTSOURCING

Selecting A Manufacturing Partner

According to KSQ’s Thomas Leitch, when it comes to selecting a manufacturing partner, company culture is as important as technological capabilities.

4 Questions To Ask Your Fill/Finish Partner

Reducing risk while maximizing API volume is critical during the fill finish phase of biopharmaceutical manufacturing. To ensure safety and quality, partner with an experienced fill finish provider.

Developing Robust mRNA Processes In A cGMP Environment

Explore current and emerging technologies to optimize mRNA manufacturing, especially when considering commercial production and the validation of processes in a cGMP environment.

Questions To Ask Your Fluid Management Component Supplier

To ensure you receive the best and safest single-use components, evaluate your fluid management supplier by asking these six questions.

6 Key Questions When Selecting Your Cell Banking Manufacturing Partner

Evaluating a potential cell banking partner's experience, testing capabilities, and approach to material management can help guarantee the quality and consistency of your therapeutic cells.

Lentiviral Vector Platform: Right The First Time

Leveraging the right LVV manufacturing platform can accelerate timelines, better manage costs, and transform product development and potential for clinical success so that therapies reach patients in need.

Project Management: The Secret Weapon In Effective Tech Transfer

Explore how a CMO with innovative practices and a successful approach to tech transfer and manufacturing processes can help meet project timelines and mitigate risk on the path to market.

CDMO Collaboration: The Foundation For Sterile Injectable Success

Leveraging a CDMO's experience with sterile injectable product development and manufacturing, as well as maintaining transparent communication, is essential to ensuring a successful product launch.

SPONSOR

Complex protein-based therapies don’t play by the same process-engineering rules as small molecules and traditional biologics. They require developers to see the unforeseen and embrace new roles and responsibilities in sourcing raw materials and outsourced expertise. Successful developers can’t let this winding road slow their time to IND. Join Bioprocess Online Live on August 8th for an interactive discussion on early workflow considerations for complex protein-based therapeutics. Supported by Thermo Fisher Scientific.

OUTSOURCING SOLUTIONS

Mammalian Cell Culture: Process R&D Services - Lonza

Link Your Antibody To Its Fullest Potential - Samsung Biologics

Seamless, End-To-End Cell & Gene Therapy CDMO - GC Cell

GMP Support For Your Media Needs - Design To Commercialization - Nucleus Biologics

Connect With Bioprocess Online: