For example companies should be compliant to 14971:2007. Design History Files need to be adjusted to meet the new standards. The FDA expects risk management to be integrated into the company quality system. Old medical devices need to have a risk assessment for each product. Each product needs to have a gap analysis to determine obsolescence or validate. It should also describe the risk acceptance criteria as well as roles and responsibilities of each member on the team.
In this webinar, we will discuss practical steps you can follow to bring your product design history files up to date with the new standards.
Areas Covered in the Seminar:
- Multi-functional team approach/responsibility.
- Set procedures and template to complete remediation for design history file of old products to meet the new standards.
- Gap analysis.
- Gathering of data to build the design history files.
- Risk procedure.
- Risk assessment for prioritizing remediation.
- Traceability matrix.
- Dealing with the FDA.
- Check list.
Who Will Benefit:
This webinar will provide valuable assistance and give a procedure to all regulated companies that need to bring their product design history files up to date with the new standards. The employees who will benefit include:
- End-users responsible for design control and technical files that need to be updated to the new standards
- R&D and product development engineers and managers
- Remediation teams
- QA, Regulatory Affairs and team members who contribute to design history or technical files
- Validation specialists
For more details:
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