In the project analysis procedures, it is of the utmost importance the discussion of URS/URD (User Requirements Specifications/Documents) that the client asks to follow.
These documents represent the starting point for a correct evaluation of our commitment to the project and for a precise verification of what will be provided.
In the pharmaceutical field, for instance, URS/URD documents are analysed in detail as they provide the basis for drafting the IQ-OQ-PQ validation documentation according to cGMP.
In the absence of URS/URD, THREAD proceeds with the drafting of these documents in agreement with the client, helping it to equip itself with this important and useful tool for both parties.