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(a) Laboratory records shall incorporate finish details derived from all assessments important to assure compliance with founded technical specs and criteria, including examinations and assays, as follows:e) Exactly where acceptable, an example or reproduction on the relevant printed packaging materials, and specimens indicating where by to apply b

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EMA Guideline on the requirements with the chemical and pharmaceutical high-quality documentation relating to investigational medicinal products in clinical trialsAt the time all of the related screening of the mobile and stationary phases are completed, which must incorporate the samples from forced degradation, even further optimization in the ch

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