Design Controls - Requirements for Medical Device Developers

The FDA expects companies to perform meaningful, results driven Design Control activities as defined in the CFR, for both new and changed devices. The company is held fully responsible for deciding when to start and the specific documentation to meet the 9 requirements. Beyond compliance, these 9 elements can be a powerful tool in reducing "time to market" - "fast cycle" product development.
For More Information Contact -
Organization: NetZealous BDA GlobalCompliancePanel
Website: www.globalcompliancepanel.com/
Email: [e-mail]
Help us caption & translate this video!
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[@carol_hyejinkim]

Great webinar. Thank you😊

[@kevinjones8488]

Great presentation! Thank you!

[@CityWalkSHA]

Still a very good training material today! Thank you!

[@imcintertech2066]

Nice video! Thanks for sharing!

[@daltonymd8391]

sterilization is definitely design output, biocompatibility aswell

[@paragkale5459]

nice

[@TeW33zy]

Didn't even understand half the words? What is the document he said download. I couldn't make out the word cusid?

[@TeW33zy]

What is cusid?

[@jlak892]

It's QSIT- Quality System Inspection Technique. Google for examples.

[@TeW33zy]

Dude before u post a video get your damn audio fixed that's crazy. People will post trash just to post

[@purpohpenguin]

Keep in mind this is a 6.5 year old video, not the newest of microphone technologies Im sure.