Insights On Pharma Logistics

31. ISO 21973: How To Ensure Full Compliance Throughout Every Step Of The Journey 6/28/2024

    Learn how ISO 21973, a vital standard for ensuring safe and reliable transport of cell and gene therapies, enhances supply chain efficiency and mitigates risks for the regenerative medicine industry.

32. BioServices: Advanced Solutions For Cell And Gene Therapy Material Management 6/28/2024

    See how supply chain solutions like BioServices can help companies mitigate risk to their overall supply chain while saving valuable capital for the research of their lifesaving therapies.

33. Safe And Compliant Shipping Of Viral Vectors In Gene Therapy 6/21/2024

    Learn about customized shippers for transporting viral vectors, the importance of comprehensive shipment monitoring, the advantages of rigorously requalifying every shipper after transport, and more.

34. Industry-Leading Advanced Therapy Support Revolutionizing Transport 6/4/2024

    Learn about a validated dry ice shipping system that fills a critical gap in the life sciences industry and is revolutionizing the transport of high-value commodities such as advanced therapies.

35. The Shift Toward Western Pharmaceutical Manufacturing 5/16/2024

    Delve into the complexities of securing and de-risking pharmaceutical supply chains in light of vulnerabilities and prompting renewed conversations about reshoring production.

36. Supply Chain Resilience 4/9/2024

    Ensure a stable and reliable supply of essential medications for patients by proactively addressing pharmaceutical supply chain challenges and embracing innovative risk management strategies.

37. Cryopreservation Best Practices For Cell & Gene Therapy Source Material 2/26/2024

    Industry experts share their experiences, including why and how cellular source materials are cryopreserved and why experience across cell types and methods matters.

38. Advancing Your API To First Human Dose Trials More Efficiently 2/7/2024

    Learn how end-to-end support for development and manufacturing, clinical trial services, advanced drug delivery, and commercial packaging can accelerate drug development and time to market.

39. Over The Hurdles: Taking Psychedelics From Schedule I To Pharmacy 10/12/2023

    Learn how a partner with experience in handling scheduled substances and navigating FDA and DEA regulation can help you advance toward clinical research and drug development with ease.

40. Could RFID-Based Unit-Level Traceability Be Key To Operational Excellence? 9/5/2023

    Radiofrequency identification (RFID)-based unit-level tracking solutions for prefilled syringes are poised to help pharma manufacturers address key risks and costly bottlenecks related to the fill-finish process.