Clinical Compliance 2011 - Presenting the real GCP handbook - Webinar By ComplianceOnline
Date2011-03-31
Deadline2011-03-31
VenuePalo Alto, USA - United States
KeywordsClinical Webinar ,conference,event.
Topics/Call fo Papers
Why Should You Attend:
When conducting a Clinical Trial, GCP is the only recognized code of practice and needs to be followed meticulously. Following patient enrollment, knowledge of GCP is taken for granted by auditors and inspectors alike. Study Sponsors, include GCP training as part of investigator meetings, prestudy and initiation visits and their own employee training programs. A number of third party organizations offer relevant seminars. Training certificates are being issued to prove GCP competency. Inspectors review vigorously sponsor and site documentation to ensure adequate training.
Yet, most presentations on GCP rely more on the presenters' experiences and interpretations of the GCP guidelines than on the actual, official text.
It is highly probable that you have been trained on GCP through hands on experience, seminars on what to watch out for, webinars on audit findings, relevant organization SOPs than from the official GCP handbook!
NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
When conducting a Clinical Trial, GCP is the only recognized code of practice and needs to be followed meticulously. Following patient enrollment, knowledge of GCP is taken for granted by auditors and inspectors alike. Study Sponsors, include GCP training as part of investigator meetings, prestudy and initiation visits and their own employee training programs. A number of third party organizations offer relevant seminars. Training certificates are being issued to prove GCP competency. Inspectors review vigorously sponsor and site documentation to ensure adequate training.
Yet, most presentations on GCP rely more on the presenters' experiences and interpretations of the GCP guidelines than on the actual, official text.
It is highly probable that you have been trained on GCP through hands on experience, seminars on what to watch out for, webinars on audit findings, relevant organization SOPs than from the official GCP handbook!
NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Other CFPs
- How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant?
- Responsibilities of a Clinical Research Coordinator managing clinical trial
- FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program
- Last changes in Canadian ethics regulations for clinical trial
- How to secure GCP compliance in Clinical Trials - Webinar By ComplianceOnline
Last modified: 2011-02-02 18:00:37