Experic recently participated in Clinical Trial Supply West Coast 2026 in Burlingame, California, connecting with pharmaceutical and biotechnology professionals focused on addressing the evolving challenges of clinical trial supply.
Representing Experic at the event were Chris Riggio, Sr. Director of Business Development, and Jerra Langit, Director of Business Development, who met with attendees to discuss the growing complexity of clinical programs and the importance of flexible, integrated approaches to clinical supply.
As clinical trials become increasingly global and operationally complex, sponsors must manage a range of interconnected requirements—from packaging and labeling to temperature-controlled storage, inventory management, and distribution. Bringing these activities together can help reduce handoffs, improve visibility, mitigate supply risks, and keep investigational products moving efficiently to clinical sites and patients.
Experic supports clinical programs through an integrated suite of clinical packaging and labeling, storage, inventory management, logistics, and global distribution services, backed by a team focused on responsiveness and adaptability as study requirements evolve.
Participation in Clinical Trial Supply West Coast provided another opportunity for the Experic team to engage directly with the clinical supply community, exchange perspectives on emerging needs, and better understand the challenges sponsors are facing as they plan and execute increasingly complex studies.
To learn more about Experic’s clinical supply capabilities, contact our team to discuss your upcoming program.