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UPCOMING LIVE SEMINARS
 






RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials

Upcoming Courses
Course #: BI11401
October 10, 2013
1:00 PM - 3:00 PM Eastern
$695.00
Course #: BI11428
December 3, 2013
1:00 PM - 3:00 PM Eastern
$695.00

Course Description

RECIST stands for Response Evaluation Criteria in Solid Tumors. The National Cancer Institute is the best resource for information, and defines RECIST criteria as “a voluntary, international standard, and not an NCI standard. They are based on a simplification of former methods (WHO, ECOG) and based on measurable disease, i.e., the presence of at least one measurable lesion.” RECIST criteria provide a way to standardize measurement of solid tumors worldwide for any clinical trials that include this data to define study endpoints.  

RECIST defines and standardizes how and when subjects are seen to progress, respond or remain stable in terms of their metastatic disease burden during a course of therapy. When these criteria are not well understood at the site level or consistently followed during a trial, it can put the study endpoint data in jeopardy.

Learning Objectives

  • Differentiate between RECIST 1.0 and 1.1
  • Describe the components of RECIST/tumor data
  • Correctly calculate TRG disease response
  • Identify and predict common trends with tumor data
  • Use working knowledge of common trends to help develop Case Report Forms for oncology trials

Who Should Attend

  • Clinical Research Coordinators
  • Clinical Research Associates
  • Clinical Team Managers
  • Primary Investigators who are interested in participating in oncology clinical trials, but who do not specialize in oncology or radiology

Instructor

Jackie Earabino, R.N., B.S.N. 

Click here for complete trainer biographies 

Registration Fees

$695

Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call 1-800-856-2556 for pricing.

Accreditation Information
 

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 2 hours (0.2 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will mail ACPE statements within three weeks of program completion. ACPE#: 0778-0000-11-030-L01-P. Released: 3/11. 

Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471. 

 

 

 

On-Demand GCP Refresher Training 

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Barnett "Hands-On" Workshops are designed to provide intensive, hands-on training in a highly targeted clinical research topic area in a very interactive and engaging learning environment. To view more details and available courses, click here.


BARNETT CATALOGThe Barnett Catalogue is your comprehensive guide to the myriad live, web, and custom training opportunities offered throughout the year. 

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Live SeminarLIVE SEMINARS

Monitoring Clinical Drug Studies: Intermediate 

Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 


Web SeminarWEB SEMINARS

10-Week CRA & CRC Beginner Program  

Trial Master File (TMF) for Sponsors: Set-Up and Maintenance 

Use of Notes to File in Clinical Trial Essential Documentation 

10-Week Clinical Research Associate (CRA) On-Boarding Program  


PublicationsPUBLICATIONS

2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)