Big Data in FDA-Regulated Industry - Best Practices for Systematic Use

Big Data in FDA-Regulated Industry - Best Practices for Systematic Use is a webinar that covers topics such as:

  • Definitions
  • Applicable Laws, Regulations, Guidance, Rules, Standards
  • Power of Big Data
  • Big Data Sources in Pharmaceuticals and Medical Devices
  • Drug Safety Data and Signals
  • Data Mining
  • Solving Big Problems Using Big Data
  • Medical Device Safety Data
  • Big Data, Security and Privacy Matters
  • Science Using Big Data
  • Revolution in FDA-Regulated Industry Using Big Data
  • Big Data v. Drug Discovery
  • Big Data: Current Trends
  • Company’s Views on Big Data
  • Big Data: Legal, Ethical and Policy Issues
  • Big Data Driven Medicines
  • Inadequate Use of Big Data
  • Failure to Use Big Data
  • Big Data: Opportunities
  • Big Data Management
  • Post-marketing surveillance
  • Big Data: Challenges
  • Speaker’s PASS-IT Suggestions/Recommendations
  • Systematic Use of Big Data: Best Practices
  • Conclusion
  • Speaker’s Experience and Actual Cases

Big Data in FDA-Regulated Industry - Best Practices for Systematic Use is intended for:

  • Regulatory Affairs Departments
  • Quality Departments
  • Manufacturing Departments
  • Research and Development Departments
  • Operations Departments
  • Engineering Departments
  • Senior Management
  • Production Departments
  • Product Development Professionals
  • Marketing Departments
  • Contractors and subcontractors
  • Clinical Affairs Professionals
  • Everyone interested in the topic
  • Consultants

Future Events

Big Data in FDA-Regulated Industry - Best Practices for Systematic Use 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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