08.06.25 -- Relationship Equity With CDMOs Is Real, Take It From A Packaging Pro

Explore the key advantages of stick-pack formats, from enhanced product safety and cost-efficiency to improved compliance and marketability.

As therapeutics continue to establish themselves as a leading technology for treating chronic indications, drug sponsors must identify reliable suppliers to secure high-quality starting materials.

Watch as experts walk through several technologies and case studies, focusing on liquid-phase peptide synthesis, crystallization, method development for impurity analysis, and more.

There are different staffing options for building an agile and scalable team that can quickly react to shifting needs, resources, and funding.

In the era of seamless development, reducing time to the clinic and getting rapid approval is key. An integrated approach can accelerate timelines, avoid communication pitfalls, and improve outcomes.

Discover a screening process to quickly assess HME feasibility that yields more accurate predictions for API loading and degradation while saving material and time compared to traditional approaches.

It is a challenge to keep improving product value for customers while reducing overall costs. Part of the solution resides in the functional activities of the risk involved and the cost of quality management.

Examine industry-leading formulation services for small molecules designed to support every stage of development—from preclinical through clinical trials to commercialization.

Early identification of potential absorption risks is critical for rapid and efficient drug development. Learn how our services can de-risk your drug development program.

Observe an innovative nanoparticle technology and the value it can bring to molecules in development or products on the market for neurological disorders.