When to Perform Installation Qualification (IQ) in Medical Device Manufacturing

Whether or not to perform an Installation Qualification (IQ) can be decided based on risk. The most important question is: Does it affect the product quality?
Watch the video for examples and explanations of why an IQ should be performed.

Do you want to learn more about Installation Qualification in MedTech? Then check out our blog article about IQ:

https://www.sifo-medical.com/post/installation-qualification

If you are unsure whether to perform an IQ, leave us a comment below!

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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 YouTube, 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).

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Related Topics:
Medical Device Consulting
Quality Management
Supplier Management
Process Validation
Operational Qualification
Installation Qualification
Performance Qualification

Видео When to Perform Installation Qualification (IQ) in Medical Device Manufacturing канала SIFo Medical – Supporting MedTech Companies