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New USP & FDA Approaches for HPLC Ensuring HPLC Data Integrity With PostConference Workshop CDS Audit Trail Review 18 May 2018SPEAKERS:Dr Markus Date F. Hoffmann Roche AG, Basel, Switzerland Dr Joachim
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New USP (United States Pharmacopeia) and FDA (Food and Drug Administration) regulations governing the quality and safety of pharmaceutical products.
Pharmaceutical companies and manufacturers are required to file under the new USP and FDA regulations.
The new USP and FDA forms can be filled out online through the respective official websites or through a compliance software.
The purpose of the new USP and FDA regulations is to ensure the quality, safety, and efficacy of pharmaceutical products in the market.
Information related to manufacturing processes, quality control measures, ingredients, packaging, labeling, and testing procedures must be reported on the new USP and FDA forms.
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