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  • Implementation and Utilization of Standard Operating
    Procedures (SOPs) at the Clinical Research Site

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Wednesday - Mar 06, 2013 10:00 AM
  • End Time:
  • Wednesday - Mar 06, 2013 11:00 AM
  • Location:
  • Online
  • This webinar will assist clinical research personnel in developing/acquiring SOPs for their site. You will learn how to create a compliant but user–friendly set of SOPs that can pass regulatory audits and also be a useful tool for the site staff.

    Why Should You Attend:

    ICH GCP guidelines require that all research sites have “Detailed, written instructions to achieve uniformity of the performance of a specific function.” Regulatory agencies are now requiring that every site have a set of SOPs for the elements of clinical research to assure compliance with ICH GCP and ask to review the site’s SOPs during audits.

    This course will cover the minimum requirements necessary for SOPs to pass a regulatory audit. It will also offer tips on streamlining the process of development and implementation of SOPs at the site level.

    Learning Objectives:

    You will learn why SOPs are required at the site level, how to develop SOPs and how to implement them.
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