Monitoring for Clinical Research and GCP Workshop
The goal will be accomplished through lecture, discussion and practical application facilitated by certified clinical research professionals with combined clinical research experience of more than 20 years. Information will be presented and discussed regarding the conduct of clinical trials; regulatory guidelines regarding IRB oversight and human research protections; ethical issues in clinical research; and workshops will stress the ability to follow directions and practices related to abstracting information and completing case report forms and other records.
|Contact No. :||215.822.8644|
Conference Fee Details
|Conference Fee||:||USD $685.00|
|Early Fee Last date||:||NA|