This spiral-bound, 5.5" x 7.5" book is a compilation of documents from various US government cancer research divisons developed to assist investigators and their site staff on conducting cancer clinical trials. It includes such topics as:
• How to write a cancer clinical trial protocol
• Developing an informed consent form
• Reporting adverse events
It also includes the latest Common Terminology Criteria for Adverse Events (CTCAE).
What's the Price?
• 1-249 copies: $18.95 • 250-499 copies: $17.95
• 500-749 copies: $16.95 • 750+ copies: $15.95
Custom Cover Prices*?
• 1-24 copies: unavailable • 25-100 copies: $2.00/book
• 100-249 copies: $1.00/book • 250+ copies: No charge
* Based on quantities of a single book title
• A Handbook for Clinical Investigators Conducting
Therapeutic Clinical Trials Supported by CTEP, DCTD, NCI
2014 (Version 1.2)
• Letter of Intent Instructions
NCI/CTEP Career Development
• Components of a Competitive Letter of Intent
Investigational Drug Branch, CTEP, DCTD, National Cancer
Institute
• Protocol Authoring and Submission Guidelines Handbook
NCI/Cancer Therapy Evaluation Program
• NCI Consent Form Template for Adult Cancer Trials
Version Date May 12, 2013
• NCI Guidelines For Investigators: Adverse Event
Reporting Requirements For DCTD (CTEP and CIP) and
DCP INDs and IDEs
Effective September 16, 2013
• NCI Guidelines For Auditing Clinical Trials for the NCI
National Clinical Trials Network (NCTN) Program,
Community Clinical Oncology Program (CCOP)/NCI Community Oncology Research Program (NCORP) and Research Bases
Clinical Trials Monitoring Branch, Division of Cancer Treatment
and Diagnosis, National Cancer Institute
• Common Terminology Criteria for Adverse Events
(CTCAE)
Version 5.0, Published: November 27, 2017
U.S.Department of Health and Human Services, National
Institutes of Health, National Cancer Institute
Click here to see an enlarged pdf cover
