New Amendments of Critical Parameters in Canadian Clinical Trials - Webinar By GlobalCompliancePanel

This presentation will help you to understand the last changes that occurred in Canadian ethics regulations. The presentation will clarify for sites and sponsors how to easy the ethics process and how to get more quicker the ethics approval. Also after the presentation the participant will understand how to apply the last changes in ethics regulation in the day-to-day work. Every member of the study team and site staff participating in the clinical trial plays an important key role. Knowledge of ethics regulations will ensure quicker ethics approval, no audit findings, speeds up the process for new drugs approval and decreases the costs to sponsors.

With the growth of the Pharmaceutical and Biotechnology industry, ethics regulations become more and more complicated. The complexity of the investigational products and of the clinical trial protocols amplified the risks for noncompliance with ethics regulations. To protect safety and liberty of clinical trial participants some of the ethics regulations changed in the last years. Also, concerns for patient’s confidentiality and privacy brought some other changes in the regulations.

Areas Covered in the Session:
New ethics regulations in Canada
Role and responsibilities of clinical trial staff
Key aspects of the role and key players involved the ethic process
Preparing protocol submission
IND safety submissions
Who Will Benefit:
Clinical Trial Sponsors Study Team
CROs Study Team / Study Managers
Clinical Team Leads
CRAs
Principal Investigators
Site Managers and Study Coordinators
New Clinical Research Coordinators
New Principal Investigators
Regulatory Compliance Associates and Managers

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884