Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial 2012

  • 12 Jul 2012
  • Webinar

Description

Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial 2012 is a webinar that covers topics such as:

  • Audit Vs. Research
  • What is clinical Audit?
  • Five stages of Clinical Audit
  • The Audit Cycle
  • What are the risks?
  • QA Program factors- implementing a program in place
  • Interactive case study to learn about audits
  • What a sponsor and investigator need to know about FDA audit?
  • Preparing for a site visit
  • Tips for a successful study
  • Most common FDA violations/actions

Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial 2012 brings together attendees from Clinical research organization, research sites, biotech and pharmaceutical industries that conduct clinical trials, including Clinical Trial staff and management, Regulatory Affairs, Project Managers, Clinical Development and Drug Safety staff.

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Important

Please, check "Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Hospitals & Clinics, Medical laboratories, Pharma
Science: Life Sciences & Biology
Technology: Biotechnology

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