Analyzing Your Biggest Data - Practical Text Mining for Regulated Companies 2014

  • 16 Jul 2014
  • Webinar

Description

Analyzing Your Biggest Data - Practical Text Mining for Regulated Companies 2014 is a webinar that covers topics such as:

  • FDA`s and EU’s emphasis
  • FDA device clearance / approval
  • Tracking and evaluating changes the "tipping point"
  • Product changes and filing a new 510(k) who`s responsible
  • The FDA`s "Decision Tree"
  • Is the process "risk based"?
  • Resolving a "wrong decision"
  • Documenting the process / rationale

Analyzing Your Biggest Data - Practical Text Mining for Regulated Companies 2014 is intended for:

  • Regulatory affairs
  • Senior management, project leaders, internal / external consultants
  • R&D and engineering staff
  • Quality systems personnel / QAE
  • New product development, regulatory submissions, driving company-wide quality initiatives, under a risk-justified approach
  • Personnel involved in Lean and Six Sigma Initiatives
  • CAPA personnel desiring to minimize post-production / life cycle, root cause investigation, and other costly problems

Past Events

Important

Please, check "Analyzing Your Biggest Data - Practical Text Mining for Regulated Companies" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Pharma
Technology: Biotechnology, Data management

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