09.25.25 -- Contamination Control Strategies For Drug Manufacturers

Discover why biological indicators are the gold standard for sterilization validation in pharmaceutical and medical device manufacturing, as well as how choosing the right one ensures safety and compliance.

Data-driven modeling techniques can enhance scale-up processes, streamline production, and help companies navigate the complexities of modern drug development with greater precision and reliability.

Devoting early-phase resources for solid form understanding and screening during a drug’s development lifecycle is critical, as doing so can help save time and resources on the path to market.

AI is revolutionizing CQV in life sciences by automating documentation, enabling real-time monitoring, and driving predictive quality to boost efficiency and compliance across validation processes.

Examine how counting efficiency and resolution impact data interpretation in critical environments like cleanrooms and pharmaceuticals.

Uncover valuable insights on transforming spray-dried dispersions into effective tablet formulations by exploring our interview with Dr. Ian Lafferty, Chief Technical Officer at Upperton.

Should you manage certain operations internally or partner with a trusted external provider? Watch experts discuss the benefits of outsourcing stability, storage, and testing.

Review a commercially-ready process capable of reproducing spray-dried dispersions with less manufacturing complexity and environmental impact, and out-designing and outperforming spray drying.

From de-risking initial processes to planning full-scale production, crucial decisions shape success. Explore four vital factors that demand careful consideration during the design phase.

Learn about how softgels are poised to facilitate innovation in the pharmaceutical industry as well as ongoing advancements in optimizing drug bioavailability through nano formulations.

Collaborating with an experienced CDMO can provide the expertise and facilities needed to navigate oral solid dose formulation complexities and ensure compliance with regulatory frameworks.

Proper packing for resin is crucial to prevent issues like cracking or channeling which can lead to process disruptions and product loss.

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”.

Watch to discover the key benefits of outsourcing your OSD production and explore real-world examples and best practices to help you streamline your processes and enhance your operational agility.