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  • 3-hr Virtual Seminar: South East Asia Regulatory Compliance
    for Life Science Products

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Thursday - Feb 21, 2013 09:00 AM
  • End Time:
  • Thursday - Feb 21, 2013 12:00 PM
  • Location:
  • Online
  • This 3-hr training on South East Asia regulatory compliance for life science products will discuss the regulatory structure and requirements for compliance with in-country regulations for pharmaceuticals, medical devices, biologics and combination products. This webinar will focus on a high-level composite of requirements in Taiwan, Hong Kong, Singapore, Malaysia, Vietnam & Thailand.

    Why Should You Attend:

    The South East Asian markets are growing in importance and interest in access to innovative products. In-country regulatory agencies are progressing in their sophistication, process development and regulatory requirements.

    Note: Japan & South Korea are not covered as they are the subject of popular companion courses entitled: South Korea: Navigating the Regulatory and Clinical Trial Environment and Japan: Navigating the Regulatory and Clinical Trial Environment

    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in listed South East Asian Countries. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies. Content will also include descriptions of the methods by which regulators process filings and registrations and what is expected in the authorization and dossier maintenance of licensed products.
  • Website:
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