Medical Devices: US Law, Regulation and Practice 2016

  • 13-14 Oct 2016
  • Four Points By Sheraton San Diego Downtown, CA, United States

Description

Medical Devices: US Law, Regulation and Practice 2016 is a seminar that covers topics such as:

  • Pre-market
    • Pre-submission meetings
    • Design control
  • What is a device
    • Regulation and guidance and the role of each
    • How can you tell if your product is a medical device
    • Determining your classification
  • The "different" products
    • IVDs and LDTs
    • Combination Products
    • Software
  • Marketing submissions
    • 510(k)
    • PMA
    • De novo
  • Post marketing
    • CAPA
    • QSR
    • Inspections
    • Reporting
    • Export for foreign markets
  • Clinical Trials
    • Other
    • IDE
    • Common problems in trial design and management
    • Export for trials

Medical Devices: US Law, Regulation and Practice 2016 brings together attendees involved or interested in:

  • Starting a company to sell health-related products
  • Non-regulatory or QA areas of medical device companies
  • Selling medical devices
  • Financing a health care company

Past Events

Important

Please, check "Medical Devices: US Law, Regulation and Practice" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Hospitals & Clinics, Medical laboratories, Medical technology

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