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PROCEDURE The test could be done either in 5 authentic containers if sufficient quantity of product or service is offered in Every single container along with the solution container may be entered aseptically (i.e., needle and syringe by means of an elastomeric rubber stopper), or in 5 sterile, capped bacteriological containers of ideal dimension i
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(2) Willpower of conformance to composed technical specs and a description of sampling and screening strategies for in-process elements. These samples shall be agent and effectively discovered.Labeling and packaging materials shall be representatively sampled, and examined or analyzed on receipt and just before use in packaging or labeling of a dru