Summary: Biologic clinical trials can be complex with many factors to consider.  Understanding your specific needs and developing a plan early on during drug development can...

Summary: Free trade zones (FTZ) in China provide clinical sponsors with specially designated areas to receive materials produced outside of China for the packaging, storage, and distribution...

Summary: Clinical trials are conducted according to a protocol, which is the master action plan for how the study will be conducted. Clinical trial protocol design can have a significant impact on the sourcing...

Summary: Clinical trial protocol design can have a significant impact on the commercial drug sourcing strategy for a study requiring comparators. Learn the appropriate level of detail to include in the study protocol...

Summary: As a worldwide clinical supply services leader, Catalent has the scale, expertise, and innovative solutions to improve efficiency and reduce your trial timelines.

Get insights on how contracting with a single service provider can offer significant benefits to the customer through integrated expertise between the formulation development teams, the manufacturing teams, clinical supply specialists, and the packaging teams.

Summary: Planning a clinical supply program? Don’t overlook primary packaging!

Summary: Securing timely and reliable commercial packaging services can be challenging for orphan, niche, and other low-volume drugs that must compete against high-volume drugs for access to finite production capacity at contract packagers This webinar describes one solution...

Summary: The trend toward crafting patient-centric clinical trials hold great promise in supporting patients’ willingness and ability to participate in important clinical research. However, for sponsors who are embracing the promise...

Summary: Different clinical trials have different supply needs and strategies. This recent Q&A article published in Pharmaceutical Technology features...