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100%: Todd Case/ Yuting Tian: An Introduction to Creating Standardized Clinical Trial Data with SAS (ISBN: 9781955977982) 2022, SAS Institute, in Englisch, Broschiert.Nur diese Ausgabe anzeigen…
100%: Todd Case/ YuTing Tian: An Introduction to Creating Standardized Clinical Trial Data with SAS (ISBN: 9781955977975) SAS Institute, SAS Institute, in Englisch, auch als eBook.Nur diese Ausgabe anzeigen…
100%: Todd Case/ Yuting Tian: An Introduction to Creating Standardized Clinical Trial Data with SAS (ISBN: 9781955977951) 2022, SAS Institute, in Englisch, Taschenbuch.Nur diese Ausgabe anzeigen…
An Introduction to Creating Standardized Clinical Trial Data with SAS
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Bester Preis: € 72,49 (vom 29.09.2022)1
An Introduction to Creating Standardized Clinical Trial Data with SAS (2022)
EN HC NWISBN: 9781955977982 bzw. 1955977984, in Englisch, gebundenes Buch, neu.
Lieferung aus: Niederlande, zzgl. Versandkosten.
An indispensable guide for statistical programmers in the pharmaceutical industry. Statistical programmers in the pharmaceutical industry need to create standardized clinical data using rules created and governed by the Clinical Data Interchange Standards Consortium (CDISC). This book introduces the basic concepts, pharmaceutical industry knowledge, and SAS programming practices that every programmer needs to know to comply with regulatory requirements. Step-by-step, you will learn how data should be structured at each stage of the process from annotating electronic Case Report Forms (eCRFs) and defining the relationship between SDTM and ADaM, to understanding how to generate a Define-XML file to transmit metadata. Filled with clear explanations and example code, this book focuses only on the essential information that entry-level programmers need to succeed. Computerboeken, Alle computerboeken, Engelse Boeken > Computerboeken > Alle computerboeken.
An indispensable guide for statistical programmers in the pharmaceutical industry. Statistical programmers in the pharmaceutical industry need to create standardized clinical data using rules created and governed by the Clinical Data Interchange Standards Consortium (CDISC). This book introduces the basic concepts, pharmaceutical industry knowledge, and SAS programming practices that every programmer needs to know to comply with regulatory requirements. Step-by-step, you will learn how data should be structured at each stage of the process from annotating electronic Case Report Forms (eCRFs) and defining the relationship between SDTM and ADaM, to understanding how to generate a Define-XML file to transmit metadata. Filled with clear explanations and example code, this book focuses only on the essential information that entry-level programmers need to succeed. Computerboeken, Alle computerboeken, Engelse Boeken > Computerboeken > Alle computerboeken.
2
An Introduction to Creating Standardized Clinical Trial Data with SAS (2022)
EN PB NWISBN: 9781955977951 bzw. 195597795X, in Englisch, Taschenbuch, neu.
Lieferung aus: Niederlande, zzgl. Versandkosten.
An indispensable guide for statistical programmers in the pharmaceutical industry. Statistical programmers in the pharmaceutical industry need to create standardized clinical data using rules created and governed by the Clinical Data Interchange Standards Consortium (CDISC). This book introduces the basic concepts, pharmaceutical industry knowledge, and SAS programming practices that every programmer needs to know to comply with regulatory requirements. Step-by-step, you will learn how data should be structured at each stage of the process from annotating electronic Case Report Forms (eCRFs) and defining the relationship between SDTM and ADaM, to understanding how to generate a Define-XML file to transmit metadata. Filled with clear explanations and example code, this book focuses only on the essential information that entry-level programmers need to succeed. Computerboeken, Alle computerboeken, Engelse Boeken > Computerboeken > Alle computerboeken.
An indispensable guide for statistical programmers in the pharmaceutical industry. Statistical programmers in the pharmaceutical industry need to create standardized clinical data using rules created and governed by the Clinical Data Interchange Standards Consortium (CDISC). This book introduces the basic concepts, pharmaceutical industry knowledge, and SAS programming practices that every programmer needs to know to comply with regulatory requirements. Step-by-step, you will learn how data should be structured at each stage of the process from annotating electronic Case Report Forms (eCRFs) and defining the relationship between SDTM and ADaM, to understanding how to generate a Define-XML file to transmit metadata. Filled with clear explanations and example code, this book focuses only on the essential information that entry-level programmers need to succeed. Computerboeken, Alle computerboeken, Engelse Boeken > Computerboeken > Alle computerboeken.
3
An Introduction to Creating Standardized Clinical Trial Data with SAS
~EN HC NWISBN: 1955977984 bzw. 9781955977982, vermutlich in Englisch, SAS Institute, gebundenes Buch, neu.
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
4
An Introduction to Creating Standardized Clinical Trial Data with SAS
~EN PB NWISBN: 195597795X bzw. 9781955977951, vermutlich in Englisch, SAS Institute, Taschenbuch, neu.
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
5
An Introduction to Creating Standardized Clinical Trial Data with SAS
DE NW EBISBN: 9781955977975 bzw. 1955977976, in Deutsch, SAS Institute, SAS Institute, neu, E-Book.
Lieferung aus: Deutschland, plus shipping, in stock.
An Introduction to Creating Standardized Clinical Trial Data with SAS: ab 42.99 €.
An Introduction to Creating Standardized Clinical Trial Data with SAS: ab 42.99 €.
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