11.08.24 -- Biopharmaceutical Fermentation Systems' Growing Role In Modern Medicine

Numerous factors impact a drug safety program, but proper management of three key elements drives success while creating a scalable drug safety model.

Explore the main inventory management challenges faced by fast-paced biotech and pharmaceutical laboratories and how they directly impact research outcomes, costs, and regulatory compliance.

Therapies are more complex, tailored, and varied than ever, and the associated amount of data is growing – which requires a new level of attention to detail.

Executives must take an early and active role in vetting potential partners, using a deeper understanding of the capabilities a CDMO should have to successfully bring a product to market.

Learn how rapid, nondestructive laser-based headspace analysis can support data generation to demonstrate the maintenance of seal integrity during deep cold storage and transport.

Explore key rheology concepts and terminology, and learn how to generate the required rheological profiles using high-performance instruments.

Product design, production methods, and supply chain can be leveraged to positively impact sustainability through effective planning.

Radiofrequency identification (RFID)-based unit-level tracking solutions for prefilled syringes are poised to help pharma manufacturers address key risks and costly bottlenecks related to the fill-finish process.

Learn about the complexities of scaling decisions to gain insights from biopharma developers and a CDMO, their mutual interest in achieving successful scale-up, and strategies to avoid common pitfalls.

The quality and effectiveness of drugs significantly depend on their packaging. Explore a wide range of leak testing methods that address package integrity challenges in the life science industry.

Review the pros and cons of marketed amorphous solid dispersions with so-far unpublished data as well as a green alternative to ASDs: best-in-class nanotechnology to manufacture nanocrystals.

Examine results from a study assessing the ability of a modern HPLC system to support manufacturing labs with the routine downstream analysis of DNA/mRNA therapeutics using SEC.

Explore an approach to developing a sterilizing-grade filter for high-concentration biologics that enabled extensive filterability trials to be conducted without needing a large quantity of product.

Discover how to select the right CDMO partner for your pharmaceutical project to navigate the evolving drug development landscape and ensure successful outcomes.

Learn about an optimized nest design for pre-fillable cartridges was designed using numerical simulation and data analytics, improving efficiency in pharmaceutical production.