Due Diligence - Quality and Compliance Aspects for Medical Devices 2015 is a webinar that covers topics such as:
- Team requirements
- Due Diligence Expectations and planning
- Red Flags of Quality / Compliance Issues
- Lessons Learned from Acquisitions
- Check List for Due Diligence
- How to categorize / prioritize Issues
- Preparing Recommendations for M&A
- Risk Management
- Preparing Action plans for post-acquisition
Due Diligence - Quality and Compliance Aspects for Medical Devices 2015 is intended for:
- Quality Engineers
- Due Diligence team members
- Compliance Managers
- Compliance Specialists
- Attorneys
- Quality Managers
- Business Leaders wishing to develop an M&A program
- Consultants and Contractors
