06.19.25 -- Addressing Human "Error" In Pharma Manufacturing

Continuous advancements in the process and payload development of ADCs and next-generation bioconjugates have the potential to progress targeted therapeutics and improve patient treatment.

Understand more about defining the spray drying process with an emphasis on specific enhancements to accommodate scale-up to commercial-scale equipment for challenging applications or molecules.

Uncover how innovative nasal drug delivery strategies can unlock faster, patient-friendly therapeutic solutions by combining smart formulation, advanced testing platforms, and rigorous evaluation.

Read about how life science manufacturers are supported in digital transformation, offering solutions for automation, data integration, and compliance to optimize operations.

Find out how cloud solutions empower businesses to achieve agility and security in their digital transformation journey, and explore key considerations and insights from real-world success stories.

These studies indicate that with a properly assembled vial containment system, good CCI performance can be achieved with stoppers of a given elastomer, independent of configuration/size, or vial style.

Ensure viral safety in your biotherapeutic manufacturing with valuable insights to guide informed decisions in virus filtration to align with both the PDA TR-41 (2022) and ICH-Q5A guidelines.

Review the optimization of the manufacturing process of a pharmaceutical intermediate, and discover how yield can be improved substantially via suitable reaction engineering.

Watch how to build a resilient supply chain to navigate today's complex environment. Expert speakers share insights on optimization, innovation, and strategic planning to meet evolving market conditions.

Whether working with small-scale formulations or preparing for commercial manufacturing, this session will provide actionable strategies to optimize development pipelines.

In the biopharmaceutical development world, Quality by Design cuts risk, streamlines processes, and speeds up regulatory approval.

Effective product development relies on strategic coordination and document control. Learn how medical writers manage collaboration risks and maintain quality using tools like document review systems.

The use of aqueous cleaning in medical device manufacturing can provide numerous benefits in terms of efficacy, minimal surface contact and reduced residue potential, and easier cleaning validation.