CSSi's Chris Trizna Included As A Contributing Author In Peter Schueler And Brendan M. Buckley's New Release "Re-Engineering Clinical Trials: Best Practices For Streamlining The Development Process"
GLEN BURNIE, Md., Feb. 17, 2015 /PRNewswire/ -- CSSi, (www.CSSiEnroll.com) the leader in patient recruitment solutions for the clinical research industry, is pleased to announce that President Chris Trizna is included as a contributing author in Peter Schueler and Brendan M. Buckley's new book, "Re-Engineering Clinical Trials: Best Practices for Streamlining the Development Process," published by Elsevier, Inc. This is the first book of its kind to offer best practices and solutions toward streamlining the drug development process to contain costs, integrate new technologies and increase efficiency.
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Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. "Re-Engineering Clinical Trials" evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and offers well-established methodologies and best practices based on real-world experiences from expert authors across industry and academia. Written for all those involved in clinical research, development and clinical trial design, this book provides a unique and valuable resource for streamlining the process, containing costs and increasing drug safety and effectiveness.
It is well-documented that slow patient enrollment is a global contributor of study delays. Likewise, retaining patients once enrolled can be equally arduous, but just as critical to the completion and success of a clinical trial. Trizna's contribution to "Re-Engineering Clinical Trials" focuses on Patient Recruitment in the 21st Century. "It was an honor to be able to contribute to this book," shared Trizna. "As individuals in the pharmaceutical industry are finding out, planning for patient recruitment and retention is an extremely complex process. Schueler and Buckley's book provides a thorough breakdown of how to approach and find best practices for streamlining the clinical trial process from development to design to implementation."
"Today's clinical trial protocols are complex with difficult to enroll criteria becoming the new standard of normal. In the 21st century we need to do a better job of engaging the patient through education of the conditions, promoting more awareness of clinical trials, and retooling our process of patient recruitment to meet enrollment timelines," added Trizna. "Patient recruitment is a complex strategy that begins with careful planning, research and budgeting."
For more information about "Re-Engineering Clinical Trials," please visit http://store.elsevier.com/Re-Engineering-Clinical-Trials/isbn-9780124202467/.
About CSSi
CSSi delivers global solutions that ensure successful enrollment, on time, every time. Through its innovative enrollment planning and full-service patient recruitment solutions, CSSi is able to reduce the costs and timelines associated with recruitment of subjects for clinical studies. CSSi is the only patient recruitment company with a worldwide team of Local Enrollment Specialists (LES), on the ground, close to sites and able to meet your study's recruitment goals on time.
For More Information
Visit www.CSSiEnroll.com, or contact Shannon Powell, Director of Marketing at Email or 443-308-5809.
Contact: Shannon Powell
CSSi
P: 443-308-5809
F: 410-553-0087
Email
www.CSSiLifeSciences.com
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