An application for registration of blood or a blood component product shall include both of the following:
(a) A protocol of the methods of production in detail that is followed in the production of the product.
(b) A sample of the label to be placed on the blood or blood component product.
(Amended by Stats. 2010, Ch. 235, Sec. 18. (AB 1709) Effective January 1, 2011. Became operative on January 1, 2013, pursuant to Sec. 28 of Ch. 235.)
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