| Starts: | Friday December 11, 2009 at 1:30pm |
|---|---|
| Ends: | Friday December 11, 2009 at 5:00pm |
| Event Type: | Training/Seminar |
| Region: | Antwerp Area, Belgium |
| Location: |
European Centre For Clinical Research Training Keizer Karellaan 576 Sint Agatha Berchem, BRUSSELS-CAPITAL REGION 1082 BE |
| Price: | 450 EUR (excl VAT) |
| Website: | http://www.eccrt.com |
| Industry: | medical practice |
| Keywords: | Gcp Requirements In Clinical Research, Gcp, Ich, Clinical, Research, Legal Regulations And Guidelines, Essential Documents Of Clinical Studies, Studies, Tips & Trics, Regulations, Good Clinical Practice |
| Intended For: | data nurses, CRA, clinical research associate, PM, project manager, doctor, medical doctor, investigator, site staff, study coordinator, study nurse, nurse, trial inspector, auditor, CTA, clinical trial administrator, study manager, site manager, line man |
| Organization: | European Centre for Clinical Research Training |
This concise course is designed for professionals who are active in clinical research. Without training on the International Conference on Harmonisation Good Clinical Practice (ICH-GCP) standards, or without experience in clinical research, professionals are not always aware of the legal regulations that govern clinical studies, including post-marketing trials.
This course focuses on the bare essentials and requirements of GCP in clinical studies. In addition, the implementation of GCP requirements is briefly explained and illustrated using examples from practice.