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Transitioning from RUO to CGMP for clinical trials

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"Transitioning from RUO to CGMP for clinical trials"

Navigating the unknown: What to expect when transitioning from RUO to CGMP

By 2030, the global biologics market is projected to grow and reach $664.7 billion. For new and emerging biopharma companies who want to be first to market, there is a huge pressure to meet regulatory requirements and clinical milestones while adhering to budget and time constraints. Preventing time-consuming and expensive pitfalls are necessary to maintaining momentum in the drug development process.

Partnering with a qualified supply chain management company can help biomanufacturers maximize limited resources by implementing robust systems and mitigating material and supply risks early in the process. A dependable supply company values transparency and proactive communication and will minimize risks and inefficiencies during the RUO to CGMP transition by providing consistent support and management of supply availability, interruptions, and lead times issues. Download this executive summary to learn more.

Offered Free by: Thermo Fisher Scientific
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