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As I hope you will see in this article, A Tale of Two Annexes. Learn From Europe? How An Emerging Biopharma Changed Its Supply Chain Methodology And What It Learned. Last week, I p.

The next step forward for RTT legislation is unclear. Maybe it is time to put politics aside and focus on patients. Acceptable Risk Reduces Clinical Development Time. The Challenge Of Scaling From 20 Sites To 200. Ensure A Smooth Start-Up In Gene Therapy Trials. The purpose of a comprehensive assessme.

February 26 - March 01, 2018. Join us in Toronto in 2018 to be involved in the key discussions that will move the industry forward. Whether your background is packaging, logistics, quality, distribution, security, supply chain management, or IT. we have something for you! What an eye opening experience. This was a great opportunity to meet and discuss pain points with industry leaders.

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Can Your Clinical Supply Chain Pass The Brexit Pressure Test? Clinical trial sponsors and clinical supply vendors must fully consider all attributes of their supply chains to ensure continuity of supply post-Brexit. This whitepaper outlines many questions that sponsors and vendors alike should ask. Avoiding Delays In Clinical Supply.