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- 2008028426 contributor B11104998.
- 2008028426 created "c2008.".
- 2008028426 date "2008".
- 2008028426 date "c2008.".
- 2008028426 dateCopyrighted "c2008.".
- 2008028426 description "Introduction and overview -- Good laboratory practices -- Pharmaceutical good manufacturing practices -- Process validation -- Documentation requirements -- Complaint investigation -- Food good manufacturing practices -- Sanitation compliance -- Medical device good manufacturing practices/quality system regulation -- Medical device reporting -- The medical device directives MDD-93/42/EEC and AIMD-90/385/EEC -- The in-vitro diagnostic device directive -- Animal welfare and the institutional animal care and use committee -- Good clinical practices -- Reports of correction and removals -- The basis of risk management -- The consequences of misconduct in FDA-regulated industries -- Summary.".
- 2008028426 extent "ix, 549 p. :".
- 2008028426 identifier "9781932828191 (pbk.)".
- 2008028426 identifier 2008028426.html.
- 2008028426 issued "2008".
- 2008028426 issued "c2008.".
- 2008028426 language "eng".
- 2008028426 publisher "Chico, Calif. : Paton Professional,".
- 2008028426 spatial "United States.".
- 2008028426 subject "344.7304/2 22".
- 2008028426 subject "Drugs Law and legislation United States.".
- 2008028426 subject "Food law and legislation United States.".
- 2008028426 subject "KF3869 .S36 2008".
- 2008028426 subject "Laboratories Safety regulations United States.".
- 2008028426 subject "Laboratory animals Law and legislation United States.".
- 2008028426 subject "Medical instruments and apparatus Law and legislation United States.".
- 2008028426 tableOfContents "Introduction and overview -- Good laboratory practices -- Pharmaceutical good manufacturing practices -- Process validation -- Documentation requirements -- Complaint investigation -- Food good manufacturing practices -- Sanitation compliance -- Medical device good manufacturing practices/quality system regulation -- Medical device reporting -- The medical device directives MDD-93/42/EEC and AIMD-90/385/EEC -- The in-vitro diagnostic device directive -- Animal welfare and the institutional animal care and use committee -- Good clinical practices -- Reports of correction and removals -- The basis of risk management -- The consequences of misconduct in FDA-regulated industries -- Summary.".
- 2008028426 title "The regulatory compliance almanac : a guide to good manufacturing, clinical, and laboratory practices / Les Schnoll.".
- 2008028426 type "text".