Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps) 2016

  • 02 Jun 2016
  • Webinar

Description

Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps) 2016 covers topics such as:

  • Regulatory recommendations regarding investigating and reporting adverse reactions
  • Background and scope of the guidance for industry released March 2016
  • What to expect when an establishment is investigating an adverse reaction
  • Investigating complaints of adverse reactions concerning HCT/Ps
  • When and how to submit reports of adverse reactions
  • Notifying and sharing information with other establishments that are known to have recovered HCT/Ps from the same donor
  • Completing form FDA 3500A (MedWatch)

Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps) 2016 brings together attendees from:

  • Quality professionals working in HCT/P establishments
  • Individuals working at the regulatory affairs of any HCT/P establishment
  • Physicians and consumers using HCT/Ps
  • Medical Director or physicians who oversee HCT/P establishments

Past Events

Important

Please, check "Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps)" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Quality assurance
Health & Medicine: Healthcare, Hospitals & Clinics, Infectious diseases, Medical laboratories, Medical technology

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