Knygos.lt klubas Knygos.lt nariams
87,70 €
-30%
Įprastai
125,29 €
An Introduction to Creating Standardized Clinical Trial Data with SAS
An Introduction to Creating Standardized Clinical Trial Data with SAS
Knygos.lt klubas Knygos.lt nariams
87,70 €
-30%
Įprastai
125,29 €
  • Išsiųsime per 12–18 d.d.
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 sh…
  • Leidėjas:
  • ISBN-10: 1955977984
  • ISBN-13: 9781955977982
  • Formatas: 19.1 x 23.5 x 1.4 cm, kieti viršeliai
  • Kalba: Anglų

An Introduction to Creating Standardized Clinical Trial Data with SAS (el. knyga) (skaityta knyga) | knygos.lt

Atsiliepimai

(5.00 Goodreads įvertinimas)

Aprašymas

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.

Knygos.lt klubas
Knygos.lt nariams
87,70 €
-30%
Įprastai
125,29 €
Kaina registruotiems pirkėjams
Prisijunkite ir už šią prekę
gausite 1,25 Knygų Eurų!?
Išsiųsime per 12–18 d.d.
Įsigykite dovanų kuponą
Daugiau
  • Autorius: Todd Case
  • Leidėjas:
  • ISBN-10: 1955977984
  • ISBN-13: 9781955977982
  • Formatas: 19.1 x 23.5 x 1.4 cm, kieti viršeliai
  • Kalba: Anglų

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.

Atsiliepimai

  • Atsiliepimų nėra
0 pirkėjai įvertino šią prekę.
5
0%
4
0%
3
0%
2
0%
1
0%
(rodomas nebus)