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A discussion of good laboratory, clinical, manufacturing and distribution practices, this text explains the regulatory developments for the US FDA and other regulatory authorities. Examples and checklists appear throughout, with a ... celý popis
Angličtina
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Anotácia knihy
A discussion of good laboratory, clinical, manufacturing and distribution practices, this text explains the regulatory developments for the US FDA and other regulatory authorities. Examples and checklists appear throughout, with an exploration of the role of quality assurance and risk management as components of pragmatic regulatory compliance.
Parametre knihy
Zaradenie knihy Books in English Computing & information technology Computer science
480.29 €
Angličtina
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