05.29.25 -- 8 Actions To Redefine Sponsor–CDMO Relationships

Learn more about spray drying, and explore case studies detailing its success as a critical tool in developing innovative and effective lung cancer therapies.

Residues from cleaning and disinfection are under increased scrutiny in cleanrooms. A new method using conductivity measurements offers a more accurate and objective way to quantify these residues.

Establishing an integrated, tailored data management strategy is core to getting the cell line development journey right.

Here, two of the more common methods for container closure integrity testing, high voltage leak detection (HVLD) and vacuum decay, are compared.

Novel technologies and therapies are helping drug developers to overcome challenges associated with the development of injectable and oral peptide formulations.

Delve into the significance of adept interpersonal leadership within your drug safety program, shedding light on the operational and financial benefits that stem from fostering a collaborative environment.

The FDA's Real-World Evidence framework addresses challenges in using Real-World Data for regulatory decisions, emphasizing data reliability, bias management, and successful case studies.

Gain insight about what questions to ask when developing a sterilization method and a critical tool that can help guide your decisions.

Watch how the landscape of pediatric dosage forms is evolving, with a focus on how ODTs are emerging as a specialized and practical drug delivery system for children.

In today's fast-paced production, precision checkweighing is crucial. Discover how smart algorithms, real-time analysis, and automation optimize performance and minimize downtime.

Supplying a fiberboard mockup allows a customer to make additional considerations before finalizing the design needed to enclose several processes requiring product manipulation in two or more “phases.”