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Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control

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Estimated Turnout

upto 100
Delegates
Based on previous editions

Editions

Oct 2021

Frequency

One-time
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"Let’s get together for live webinar"
Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process .. Read more Activities “on Wednesday Oct 27, 2021 03:00PM Duration: 90 Minutes. This training program will provide the regulatory requirements (US) for complaint handling in the medical device and pharmaceutical industries. The course will touch on complaint sources, and details will be furnished on the interrelationships regarding complaint handling/change control/adverse event reporting/and recalls. The course will also include timeline requirements associated to adverse event reporting, which reporting formats to use, when to recall and types of recalls. Why Should You Attend:The session will include requirements for complaint files and key requirements of:Complaint proceduresInvestigationsWhat to document when it is determined that an investigation is not needed

Highlights

  • Areas Covered in the Webinar: Complaint definition
  • Medical device and drug complaint handling requirements (US)
  • What may trigger a recall during the complaint investigation
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199 USD Participant
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Compliance.world

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