TOP 5 INSIGHTS IN CLINICAL SUPPLY CHAIN & LOGISTICS
SEPTEMBER EDITION
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A new industry group — the Cell&Gene Foundry — argues it’s time to reframe the conversation around risk, not phase. Explore why “risk-appropriate” strategies are the key to smarter automation, analytics, and scalability.
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As early phase clinical trials become more sophisticated, explore how sponsors are now leveraging flexible IRT solutions to replace error-prone manual processes and gain greater control and efficiency.
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Learn why choosing the right CDMO partner for a biotech product isn’t about “capacity at a good price”; it’s about a partner with the right mix of technical expertise, regulatory track record, and more.
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During clinical trials, the intricacies of financial management intensify, necessitating advanced ERP functionalities to handle clinical accruals, compliance, and reporting. Discover how to make smarter tech decisions at every growth stage
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Consultant Jessica Cordes provides an update on proposed changes to GMP guidance that affect trial conduct, including documentation, computerized systems, and the use of AI.
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