How we should calculate SSR value from Dissolution data sheet..? and what it indicates in actual terms ?
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What is the limit for friability of tablets?
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What do you mean by validation, whats are the different steps of validation? whats are the steps followed in process validation?
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what is manual integration in HPLC
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at what interval Ukrainian audit will come once you register your product??
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What is limit of uniformity of content as per USP?
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