full-board WCG IRB meetings each week 1-2 business days for minimal risk studies 1 business day for multi-site study review 55+ years’ experience in independent ethical review It started 55+ years ago with a focus to make ethical review better. Today, WCG does it best. ...
full-board WCG IRB meetings each week 1-2 business days for minimal risk studies 1 business day for multi-site study review 55+ years’ experience in independent ethical review It started 55+ years ago with a focus to make ethical review better. Today, WCG does it best. ...
full-board WCG IRB meetings each week 1-2 business days for minimal risk studies 1 business day for multi-site study review 55+ years’ experience in independent ethical review It started 55+ years ago with a focus to make ethical review better. Today, WCG does it best. ...
full-board WCG IRB meetings each week 1-2 business days for minimal risk studies 1 business day for multi-site study review 55+ years’ experience in independent ethical review It started 55+ years ago with a focus to make ethical review better. Today, WCG does it best. ...
Ensure robust human subject protections and compliant study conduct with reliable institutional review board (IRB) services and extensive therapeutic expertise.
Ensure robust human subject protections and compliant study conduct with reliable institutional review board (IRB) services and extensive therapeutic expertise.
Ensure robust human subject protections and compliant study conduct with reliable institutional review board (IRB) services and extensive therapeutic expertise.
Some clinical research endeavors may be exempt from IRB review, some studies able to undergo expedited review, but must will go through a full board review. There are four phases of human clinical research: phase I dose finding (20–100 subjects), phase II assessing safety and efficacy (100...
NEED AN IRB? Generally, if you have human subjects in your study, you will need IRB approval of the protocols for their protection prior to conducting your research… > Learn More IRB PROCESS There are three types of IRB review: Full Board IRB, Expedited IRB and IRB Exemption. We will he...
NEED AN IRB? Generally, if you have human subjects in your study, you will need IRB approval of the protocols for their protection prior to conducting your research… > Learn More IRB PROCESS There are three types of IRB review: Full Board IRB, Expedited IRB and IRB Exemption. We will he...