QP Roles and Responsibilities
What is the legal basis of the QP?
What differences would there be if it was a clinical trials batch?
What are the legal duties of a QP?
What are the common pressures on the QP?
Why do you want to become a QP?
What qualities should a QP have?
How should a QP handle pressure from senior management?
How do you intend to keep up to date?
What are the key qualities of a QP?
What are legal and routine duties of QP?
What are the responsibilities of QP once product has left site?
What extra difficulties are experienced by locum or contract QP’s?
Are there any guidelines for locum or contract QP’s?
Where would you find the routine duties of a QP listed?
What EC directive introduced the concept of the QP?
Give me some examples of important directives QP needs to know in detail?
As a QP what sort of things would you get involved in during an inspection?
Who is the QP responsible to?
What is in the QP code of practice?
What is different in the revised QP code of practice?
If another QP has approved part of the production process but you are doing the final release, would that affect what checks you carried out?
If more than one QP is involved with different stages of manufacture where does the final responsibility lay?