Live Webinar
on
New Amendments of Critical Parameters in Canadian Clinical Trials
Date & Time: Thursday, December 15, 2011
10:00 AM PST | 01:00 PM EST
Duration: 60 Minutes
Instructor: Calin Popa
Location: Online
Price : $245.00
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(for one participant)
Instructor Profile:
Overview:
Calin Popa Director, Advanced Clinical Research Services Inc
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.
Areas Covered in the Session: l
New ethics regulations in Canada
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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
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Click here to register for this webinar
Calin Enea Popa, MD, CCRA is the Founder and President of Advanced Clinical Research Service Inc. a Canadian full-service CRO that provides CRO services and training to FDA and Health Canada regulated industries. He provides ICH-GCP training and training for FDA and Health Canada regulations. He provides consulting services for the purpose of compliance review, drug accountability, site management, safety review, training site personnel, and to assure the integrity of clinical data. Performed site audits and site audit preparation. ...more
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Who Will Benefit: l l l l l l l l l
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
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