International reference documents serve as a valuable resource for those involved in the development, manufacturing, and use of plasma-derived therapies. These documents provide guidance on best practices and standards of care, drawing upon the collective expertise of experts from around the world. Reference documents may cover a range of topics, including the manufacturing and quality control of plasma-derived products, the selection of donors, and the screening and testing of plasma. By consulting international reference documents, healthcare providers and manufacturers can ensure that they are following the most up-to-date and evidence-based practices in the field of plasma-derived therapies.

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