Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements 2017

  • 1695.00 Dollar US$
  • Published date: April 24, 2017
    • Zurich, Switzerland, Zurich, Switzerland, Switzerland

Course "Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
• Defining the basic requirements of Good Clinical Practices
• Clinical Study Protocol Elements and Device Accountability
• Role of Institutional Review Board (IRB) and Informed Consent
• Principles of Ethics and Quality Control
• Determining the appropriate duties and oversight required of the sponsor, monitor, and investigators to ensure a high level of quality in a clinical trial
• Ensuring that quality practices are designed and implemented to guarantee compliant clinical trials
• Learning how to effectively manage a Sponsor, as well as, an FDA GCP inspection
• Developing mechanisms to uncover and preclude fraud and misconduct in clinical trials
• And Much More...

Why should you attend:
• What is GCP and why is it needed?
• History and development of GCP in EU and US and where are we now?
• Managing problem areas of working with GCP regulations and guidelines
• Impact of GCP globally and key FDA differences
• Recognize the regulatory pathways in the U.S
• Explore practical aspects of investigator and monitor selection
• Discuss how to comply with the fundamentals of Good Clinical Practice (GCP)
• Examine practical aspects of conducting international clinical trials
• Understand the significance of Ethics and Human Subject Protection
• Understand how to prepare for audit and inspection of clinical trials
• Recognize what prompts an FDA audit
• Learn how to plan for an audit or inspection, including using appropriate checklists
• Appreciate how to prepare for audit/inspection Interviews
• Consider how to respond to the audit/inspection findings
• How to monitor clinical trials effectively and efficiently
• Comprehensive overview of the applicable regulations on good clinical practice and clinical trials
• Attendees are encouraged to discuss GCP work related activities associated with their functional area on the various topics as applicable for interactive group discussion
• Review and discuss pain points, challenges and solutions

Location: Zurich, Switzerland Date: June 15th & 16th, 2017 and Time: 9:00 AM to 6:00 PM

Venue: Hilton Zurich Airport
Address: Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland. +41 44 828 50 50
Price:

Register now and save $200. (Early Bird)
Price: $1,695.00 (Seminar Fee for One Delegate)
Until May 10, Early Bird Price: $1,695.00 From May 11 to June 10, Regular Price: $1,895.00

Register for 5 attendees Price: $5,085.00 $8,475.00 You Save: $3,390.00 (40%)*


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Phone: 1-800-447-9407
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Email: john.robinson@globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com

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