Do I have to validate manual processes in medical technology?
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- Опубликовано: 11 май 2023
- Are you working in the MedTech industry and are unsure about whether you have to validate manual processes?
In this video, you'll find the answer!
If you want to learn more about Quality Management in MedTech, check out our blog articles:
www.sifo-medical.com/blog
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At SIFo Medical, we are passionate about empowering MedTech companies in Quality- and Supplier Management. From our base in the Austrian Alps, we provide MedTech manufacturers with our expertise in Quality Management, especially with:
- Compliant Technical Documentation
- Internal & External Audits
- Test Method Validation
- Product Development
- Process Optimization
- Packaging Validation
- Process Validation
- Risk Management
- Design Control
- Statistics
On RUclips, our experts provide short, informative, and easy-to-digest videos about medical device Quality- and Supplier Management to support MedTech manufacturers to produce safe medical devices and comply with necessary regulations and standards (like ISO 13485, MDR 2017/745 or FDA requirements).
Expand your knowledge in MedTech and profit from countless hours of practical expertise in the medical device industry.
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Website: www.sifo-medical.com
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Process Validation
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Process Validation in Manufacturing
Requirements of Process Validation
Stages of Process Validation
MedTech Process Validation
Operational Qualification Sample Size
Operational Qualification Requirements
IQ OQ PQ
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