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In the event that You re-enter or reprocess any Card transaction that was the subject of a Chargeback, You are solely responsible for all claims, causes of action, liabilities, and damages arising out of or relating to that transaction. 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GW hereby agrees that it will not use any material for NOVARTIS that does not meet specifications after testing.\n7.5.2. Reprocessing of intermediate drug product and drug product by an appropriate and authorised procedure after evaluation of the risks involved is only allowed in exceptional cases and is in the registered method of manufacture, provided that material is suitable for such a process and the resulting Product meets its specifications with no significant changes in Product quality.\n7.5.3. Where reprocessing is required, NOVARTIS will be informed prior to reprocessing, and the instructions to perform such reprocessing shall be documented into the appropriate master production records.\n7.5.4. NOVARTIS does not permit any rework of products or product intermediates in the sense of performing process steps that are different from the agreed manufacturing process, such as using different solvents or changing the batch size outside of +/- 10% of registered size.\n7.5.5. 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Reprocessing directions must be established to define the process. If the Product is registered, reprocessing parameters must be validated, submitted, and approved prior to implementation and batch release. 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Typically, this clause outlines the conditions, limitations, and responsibilities for reprocessing, such as quality standards, notification requirements, or cost allocation between parties. Its core practical function is to ensure that both parties understand when and how reprocessing is permitted, thereby preventing disputes over product quality, liability, or additional expenses that may arise from reprocessing activities."}, "json": true, "cursor": ""}}