11.14.24 -- CDMO Selection: 7 Steps To Find Your Best Fit

Picking and sticking are the most common tablet defects that can reduce your product quality and performance. This makes perfecting the right pre-picking strategy essential to improving your processes.

Biosimilars hold the potential to transform patient care by reducing the cost of biologic therapies. Learn about the complex path to FDA approval for biosimilars.

Explore some of the major challenges that medical writing submission specialists face today and strategies that can consistently set the stage for success.

By leveraging the expertise of CDMOs, pharmaceutical firms can expedite their time to market, reduce costs, and improve patient outcomes, ultimately advancing the future of drug delivery methods.

Understanding the transport phenomenon in the boundary layer can allow us to engineer the flow to manage the rate-limiting step and intensify the process.

Failure to identify a compound’s red flags early in development often manifests as program delays or failures. Discover how to avoid these setbacks through complete molecular characterization.

Medical and pharmaceutical products are often packaged in fluid-filled containers. Learn about CCIT using high voltage leak detection (HVLD), how HVLD technology works, and more.

The right data management platform can streamline biopharma technology transfer by bridging digital gaps, accelerating commercialization, ensuring compliance, and reducing costs.

Explore best practices to help you maximize the benefits of using software that improves efficiency in test execution documentation, contributing to a more streamlined laboratory operation.

Learn how transferring a batch chromatography process into a multi-column format and scaling that process up to continuous perfusion dramatically reduced protein A resin requirements.

Explore high shear mixers and how they can be used in a variety of ways to create cannabis-infused products.

‘Brick dust’ compounds require additional steps if spray drying is to yield a commercially attractive process. Examine three enabling technologies designed to improve drug solubility in organic solvents for spray drying.

Selecting the right CDMO to properly execute your tech transfer is critical for ensuring optimal process reproducibility that preserves the intended quality, efficacy, and safety of a drug product.

Join product and application experts Anne-Grit Klees, Carine Krebs, and Esther Welterlin to discover the benefits of using a new rapid microbial detection platform.

Understanding the obstacles you may face during bioconjugate development, as well as the tools available to help overcome them, can help streamline your product’s path to market.