-Pukar Ratti, MSChE, MSHCM, CIM, CCRP, FACMPE
System Director, Research & Academics Institutional Official
“A standard for the design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate, and that rights, integrity, and confidentiality of trial subjects are protected.” -ICH Ed 1.24
The GCP lectures are focused on up-to-date and relevant information that researchers need to conduct quality, safe, and ethical research. There are at least 6 credit hours of GCP offered annually by the CHRISTUS Health IRB. Please email the CHRISTUS Health IRB to be added to the GCP notification email list at CHRISTUS.IRB@christushealth.org.
All researchers must complete CITI training at the onset of their research. The initial CITI training requirement will expire three years after the initial year the course was completed. During the three year period (prior to the expiration date), researchers can remain certified through completion of one of the following:
*There are at least six credit hours offered annually. At least four credit hours/year for three consecutive years need to be earned to qualify.
For more information on CITI or for a CITI account please click here.
This annual two-day on-site event offers a unique learning opportunity to all members of IRB’s panel and office staff. The major highlights of this educational event are:
For more information on the IRB member annual conference, please contact the CHRISTUS Health IRB.
Please click on the links below to download the provided resources.
