Journal of Clinical Research Best Practices
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Table of Contents
Should You Be a Clinical Research Principal Investigator?
Abandon all illusions ye who enter here
Data & Safety Monitoring Boards in Industry-Sponsored Clinical Trials
When DSMBs make sense, and when they don't
18 Subject Injury and Indemnification CTA Loopholes
Who says CTA drafting isn't fun?
The Telephone Translation Game: An Illustration of Translation Challenges
How garbled are your informed consent form translations?
Season’s Greetings from Your IRB
If IRBs supervised Christmas
STRATEGIC RESEARCH: A Practical Handbook for Phase IIIB and Phase IV Clinical Studies: Chapter 6. Maximizing Value
Part 7 in a 15-part series about late-stage research
Review: “Standard Operating Procedures for Clinical Research Sites”
Everyone needs SOPs
Review: “Writing and Enforcing Effective SOPs”
SOP how-to's and why's
Review: “On the Take: How Medicine’s Complicity with Big Business Can Endanger your Health”
Let's be friends
Update on MAGI, the Model Agreement Group Initiative
Good Clinical Practice Q&A: Focus on Study Records
You too can be a GCP expert
Spotlight on Research Fees: Unique Procedures per Subject
How many is too many?
First Clinical Research Stock Index (FCRI)
Another interesting year
Mayne Cartoon Research Laboratories
FCA inspected and approved
What am I Missing Here? Thought-Provoking Questions for the Clinical Research Industry
Site monitoring visits