Regulatory Documentation in Clinical Research-BIBLE for CRO & CRA

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9781515022862: Regulatory Documentation in Clinical Research-BIBLE for CRO & CRA
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This book entitled “Regulatory Documentation in Clinical Research-BIBLE for CRO & CRA“ is a must read book for aspirants who are engaged in Clinical Research Documentation Preparation as they have to survive in workplace of stricter regulations and statutory compliances. This is a complete textbook on the subject matter and covers the general topic on the writing of various regulatory documents eg.Study Protocol, Investigator’s Brochure (IB) & Clinical Research Study Report (CSR) etc. The book is a continuous effort of the author to provide the knowledge and guidance involved in the field of Clinical Research and regulatory documentations. The book summarizes how to write these documents with ease and every step is explained in detail. There is also glossary of terms and Abbreviations given- in which detailed supporting reading material has been provided.

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Kanosia
ISBN 10 : 1515022862 ISBN 13 : 9781515022862
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Description du livre Paperback. État : New. This item is printed on demand. Item doesn't include CD/DVD. N° de réf. du libraire 8648821

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Kanosia
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Description du livre 2015. PAP. État : New. New Book.Shipped from US within 10 to 14 business days.THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. N° de réf. du libraire IP-9781515022862

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Kanosia
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ISBN 10 : 1515022862 ISBN 13 : 9781515022862
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Description du livre Createspace Independent Publishing Platform, United States, 2015. Paperback. État : New. 280 x 216 mm. Language: English . Brand New Book ***** Print on Demand *****.This book entitled Regulatory Documentation in Clinical Research-BIBLE for CRO CRA is a must read book for aspirants who are engaged in Clinical Research Documentation Preparation as they have to survive in workplace of stricter regulations and statutory compliances. This is a complete textbook on the subject matter and covers the general topic on the writing of various regulatory documents eg.Study Protocol, Investigator s Brochure (IB) Clinical Research Study Report (CSR) etc. The book is a continuous effort of the author to provide the knowledge and guidance involved in the field of Clinical Research and regulatory documentations. The book summarizes how to write these documents with ease and every step is explained in detail. There is also glossary of terms and Abbreviations given- in which detailed supporting reading material has been provided. N° de réf. du libraire APC9781515022862

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Kanosia
Edité par Createspace Independent Publishing Platform, United States (2015)
ISBN 10 : 1515022862 ISBN 13 : 9781515022862
Neuf(s) Paperback Quantité : 10
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The Book Depository US
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Description du livre Createspace Independent Publishing Platform, United States, 2015. Paperback. État : New. 280 x 216 mm. Language: English . Brand New Book ***** Print on Demand *****. This book entitled Regulatory Documentation in Clinical Research-BIBLE for CRO CRA is a must read book for aspirants who are engaged in Clinical Research Documentation Preparation as they have to survive in workplace of stricter regulations and statutory compliances. This is a complete textbook on the subject matter and covers the general topic on the writing of various regulatory documents eg.Study Protocol, Investigator s Brochure (IB) Clinical Research Study Report (CSR) etc. The book is a continuous effort of the author to provide the knowledge and guidance involved in the field of Clinical Research and regulatory documentations. The book summarizes how to write these documents with ease and every step is explained in detail. There is also glossary of terms and Abbreviations given- in which detailed supporting reading material has been provided. N° de réf. du libraire APC9781515022862

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Description du livre CreateSpace Independent Publishing Platform. Paperback. État : New. This item is printed on demand. Paperback. 160 pages. Dimensions: 11.0in. x 8.5in. x 0.4in.This book entitled Regulatory Documentation in Clinical Research-BIBLE for CRO and CRA is a must read book for aspirants who are engaged in Clinical Research Documentation Preparation as they have to survive in workplace of stricter regulations and statutory compliances. This is a complete textbook on the subject matter and covers the general topic on the writing of various regulatory documents eg. Study Protocol, Investigators Brochure (IB) and Clinical Research Study Report (CSR) etc. The book is a continuous effort of the author to provide the knowledge and guidance involved in the field of Clinical Research and regulatory documentations. The book summarizes how to write these documents with ease and every step is explained in detail. There is also glossary of terms and Abbreviations given- in which detailed supporting reading material has been provided. This item ships from La Vergne,TN. Paperback. N° de réf. du libraire 9781515022862

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Kanosia
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Description du livre 2015. PAP. État : New. New Book. Delivered from our US warehouse in 10 to 14 business days. THIS BOOK IS PRINTED ON DEMAND.Established seller since 2000. N° de réf. du libraire IP-9781515022862

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