Jump to content

Ortho BioVue


tamam

Recommended Posts

khalidm3 -

We do what David described.

Do you have some agency requirement that you check the potency/Titre of the antisera, or is that simply a policy for your own facility? Assuming that you have done those checks for several years, what have you found in the past? Do many of your reagents fail the potency/Titre checks that you do? (And what do you do if/when they fail?)

Donna

Link to comment
Share on other sites

It is required by the MOH, to validate all lots, Our central stores do not issue any reagent till it is evaluated. My centre is the evaluating centre for this area.

Years ago Anti c anti sera, failed, the titre proved less than 2, even with double dosage. The manufacturer (a Canadian firm) took back the shipment. Sometimes we rejected substandard disposables too (local firms). We rejected pricing pens to be used for multiple patients/donors. Long long ago we rejected a Glucose metre, whose results were substandard (US firm-at that time I was not in BB). Might be some more examples also

Link to comment
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Recently Browsing   0 members

    • No registered users viewing this page.
  • Advertisement

×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.