Excellence Beyond Compliance Establishing A Medical Device Quality System

William I. White

Excellence Beyond Compliance Establishing A Medical Device Quality System - 1
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Excellence Beyond Compliance Establishing A Medical Device Quality System
Many companies limp along from day-to-day treating the quality side of the business as a necessary evil, and doing only what is minimally necessary for compliance to regulations. This kind of approach to compliance almost always results in inefficiencies and sometimes can result in a curious kind of noncompliance. Documentation created with compliance as the sole consideration often ends up confusing the employees who must use the documentation....

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Resumo

Excellence Beyond Compliance Establishing A Medical Device Quality System

Many companies limp along from day-to-day treating the quality side of the business as a necessary evil, and doing only what is minimally necessary for compliance to regulations. This kind of approach to compliance almost always results in inefficiencies and sometimes can result in a curious kind of noncompliance. Documentation created with compliance as the sole consideration often ends up confusing the employees who must use the documentation.

This book looks beyond what is necessary for compliance alone to address what makes a quality management system (QMS) both effective and efficient. This book also never forgets that real people must make any QMS work, the book provides a blueprint for creating a QMS that real people will find useful.

After a review of the challenges that any medical device company faces in the world of todayâthe multiple sources of QMS requirementsâthe book poses a question: are we satisfied with the QMS we have now, or could we do better? If we want to do better, this book can help.

This book offers:

  • Advice that will lead to an effective and efficient QMS.
  • Detailed guidance on the key decisions to be made regarding the quality system being established.
  • Detailed ideas on how to execute those decisions.
  • Up-to-date information on compliance to current regulations and standards and guidance on staying up to date.
  • Specific examples of procedures.
  • Information regarding requirements for combination products, such as a drug + device combination.
  • Advice on incorporating risk management in the QMS.

Nº de Páginas: 236
Encadernação: Capa Dura / Hardback
Tema: Other manufacturing technologies
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Características

Editora

Taylor & Francis

Idiomas

Inglês

Número de páginas

236,0

Peso

600,0

Colecção

Other manufacturing technologies

Data de lançamento

24/05/2018

Série/Edição Limitada

1

EAN

9781138491472

Publicidade
Publicidade