Cra's Guide to Monitoring Clinical Research

Cra's Guide to Monitoring Clinical Research
- Used Book in Good Condition
The CRA's Guide to Monitoring Clinical Research, now in its third edition, continues to be a key resource for both novice and experienced CRAs seeking to learn more about the field of monitoring or to better understand their roles and responsibilities as the industry becomes more global and technologically focused. With helpful tips and strategies, checklists, personal experiences, key takeaways and exercises, plus new chapters on clinical trial roles and responsibilities, monitoring for device and biologic trials, globalization of studies, EDC and more, The CRA's Guide is a must-have training and educational tool that you ll refer to again and again.

Topics include: -A comprehensive review of CRA roles and responsibilities
-Understanding regulations and GCPs
-Study initiation and monitoring plans
-Recruiting and retaining study subjects -The informed consent process
-Conducting adverse event and safety monitoring
-Preparing for audits and detecting fraud
-The future outlook
-Job descriptions and current academic programs
-Devices and Biologics
-Managing Multi-national Trials
-IRBs and Data Safety Monitoring Boards
-Exercises with Answers

Recommended for: -Novice and experienced CRAs
-Health professionals interested in pursuing a career as a study monitor
-Instructors conducting training and educational programs
Country USA
Brand Brand: CenterWatch
Manufacturer Centerwatch Inc
Binding Paperback
EANs 9781930624603
ReleaseDate 0000-00-00

Country	USA
Brand	Brand: CenterWatch
Manufacturer	Centerwatch Inc
Binding	Paperback
EANs	9781930624603
ReleaseDate	0000-00-00

Cra's Guide to Monitoring Clinical Research

You might also like...