Patient Registry Data for Research: A Basic Practical Guide
Analysis of patient data can be a complicated and challenging process, especially when the data involve many subjects and many variables. A patient registry is a database that organizes collecting the important set of data on a list of identifiable individuals for a specific disease. This type of data usually has tons of data and hundreds of different variables. Thus, the approach to conducting research by using a patient registry database will be more complicated than the other types of dataset. Since the handling of patient registry data is a challenging task, the authors have come out with this e-book/book to become a guideline for the statisticians, medical officers and scientists for them to refer as a handbook whenever they need to use patient registry data for their research.
About Author:
Dr. Mohamad Adam Bujang is a Senior Research Officer at the Institute for Clinical Research (ICR), Ministry of Health, Malaysia shared his many years of experience in conducting medical research consultation in this short, concise e-book. Now, it is available for free at your favourite e-book store.
Read online (Flipbook)
NIH Library: http://library.nih.gov.my/e-doc/flipbook/
Download via:
Books2Read (list of online Book Stores): https://books2read.com/u/brP99w
Smashwords: https://www.smashwords.com/books/view/1081641
