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RAW MATERIAL RISK ASSESSMENTS - BioPhorum

RAW MATERIAL RISK ASSESSMENTS - BioPhorum

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2 ICH Q7, Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients, Section 1.3, Scope 3 EU (2015/C 95/02), Guidelines on the formalised risk assessment for ascertaining the appropriate good manufacturing practice for excipients of medicinal products for human use, Chapter 2.3

  Assessment, Good, Practices, Pharmaceutical, Manufacturing, Active, Ingredients, Risks, Material, Good manufacturing practice, For active pharmaceutical ingredients, Raw material risk assessments

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