Seeking TEG 6S Validation Plan & Supporting Documents
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We’re in the process of developing a validation plan for two TEG 6S analyzers that we’ll be implementing. I’ve reviewed several helpful posts here already, but I was wondering if anyone would be willing to share their full validation plan as a reference?
This device is new to me, so I’m still learning. For those who have implemented TEG 6S, did you use the reference ranges provided by the vendor, or did you establish your own?
Additionally, we likely won’t be able to go live with an interface until sometime in 2027, so we’ll be starting with a paper-based workflow. If anyone has procedures, QC logs, or other documentation they’d be willing to share, I’d be incredibly grateful.
Thanks in advance for your support!
This device is new to me, so I’m still learning. For those who have implemented TEG 6S, did you use the reference ranges provided by the vendor, or did you establish your own?
Additionally, we likely won’t be able to go live with an interface until sometime in 2027, so we’ll be starting with a paper-based workflow. If anyone has procedures, QC logs, or other documentation they’d be willing to share, I’d be incredibly grateful.
Thanks in advance for your support!
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If I can find our validation plan, I could share that too.
Thank you for all that have sent me documentation-it has been very helpful!