A
Hi,
we have received an info on a raw material we use which says that the products status has changed from "tested" to "listed" in the EU Pharmacopoeia.
The memo didn't mention what will be the consequences to the raw material on this change.
Can anyone explain me what changes/consequences this change of the materials status brings ?

we have received an info on a raw material we use which says that the products status has changed from "tested" to "listed" in the EU Pharmacopoeia.
The memo didn't mention what will be the consequences to the raw material on this change.
Can anyone explain me what changes/consequences this change of the materials status brings ?
