The emergence of cell and gene therapies (CGTs) represents a paradigm shift in modern medicine, offering unprecedented potential for treating previously incurable diseases.
However, the advance of these groundbreaking therapies brings forth a myriad of logistical challenges, particularly in the management of complex samples. As the CGT landscape rapidly evolves, clinical research companies face the critical task of navigating intricate supply chain management and transportation processes while safeguarding proprietary information vital for innovation and competitiveness.
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