Big Data in FDA-Regulated Industry - Best Practices for Systematic Use 2019 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 2019 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
