Before Your Trial Goes Live – InForm FastStart

When EDC is used in a clinical trial, electronic case report form (e-CRF) data are defined to be the data that are manually entered into a computer by the patient or by the investigator’s staff. CDISC defines e-CRF as a CRF in which related data items and their associated comments, notes, and signatures are linkedContinue reading “Before Your Trial Goes Live – InForm FastStart”

How to Manage Sites and Users in InForm Trial?

So you created your first InForm Trial and now what? Before you can actually enter data into your trial, you need to set up a user management system which assigns permissions to different users in your system depending on their job “role”. In InForm, this is accomplished by using a tool called ‘User Management Tool’Continue reading “How to Manage Sites and Users in InForm Trial?”

Data Management Plan in Clinical Trials

  The preparation of the data management plan (DMP) is a simple, straightforward approach designed to promote and ensure comprehensive project planning. The data management plan typically contains the following items. They are: Introduction/Purpose of the document Scope of application/Definitions Abbreviations Who/what/where/when Project Schedule/Major Project Milestones Updates of the DMP Appendix The objective of thisContinue reading “Data Management Plan in Clinical Trials”

Reasons I Like My Job

It has been a little while since my last blog. I have been busy this summer with the acquisition of a new member of our family – a 7 weeks-old White Westie. I have been most of the summer taking him to the park, riding the bike to the local beach or lake in hisContinue reading “Reasons I Like My Job”