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Clinical Trial Labeling - What Does Compliance Look Like and How Does the Pharmaceutical Industry Best Manage It?

Overview


This Solution Provider Webinar is brought to you by DIA in cooperation with Lionbridge Life Sciences


This on demand webinar will take approximately 1 hour to complete


This webinar will address the management and compliance associated with Clinical Trial labeling, across all regions, countries, and health authorities. We will discuss how stakeholders across the pharmaceutical industry should approach these issues, and best practices for making the process as streamlined and straightforward as possible. The webinar will also stimulate discussion on the topics covered, allowing you to share best practices and thoughts for the successful management of clinical trial labeling.

Featured topics

  • Regulatory information on clinical labels
  • Label formatting and presentation
  • Access to country regulations
  • Building, managing, and maintaining a clinical labeling phrase library
  • Regulatory requirements and the review process
  • Considerations for translation
  • Process optimization through technology and by minimizing touchpoints
  • Who should attend?

    Professionals who work in the area of:
    • Clinical Operations
    • Clinical Vendor Management
    • Clinical Trial supply chain
    • Packaging operations

    Learning objectives

    At the conclusion of this on demand webinar, participants should be able to:
    • Define the options and approaches to clinical trial labeling management
    • Discuss ideas for best practices in the area covered
    • Recognize areas for process improvement and simplification

     Continuing Education Credits are not available for this event.

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