Clinical Site Coordinator / Manager and GCP Workshop
The goal will be accomplished through lecture and practical application facilitated by clinical research professionals with a combined industry experience of more than 20 years. Information will be presented and discussed regarding administration of clinical trials according to FDA Regulations and International Conference on Harmonisation (ICH) guidelines as well as practical procedures and site/sponsor /CRO relationships.
|Contact No. :||(312) 787-2900|
Conference Fee Details
|Conference Fee||:||USD $690.00|
|Early Fee Last date||:||NA|