as of 2019 - 03 - 18

14.A Sampling

14.A Sampling
Here you will find answers to the following questions:

Why is sampling classified as a critical process step?

What regulatory requirements are to be upheld during sampling?

What requirements are placed on the sample taker, the rooms and the environmental conditions?

What equipment is necessary to ensure a representative sample?

Which materials are to be sampled and what factors are to be considered?

How can factors influencing the sampling process be determined as part of a risk assessment?

How does one determine a representative sample size?

What methods are there for drawing samples?

What are the basic rules for ensuring that representative samples are taken?

What requirements are placed on the documentation?

What must be considered regarding the subsequent storage and shipment of the samples?

How does a microbiological sample procedure differ from a sampling for chemico-physical characterization?

A paid subscription is needed to login into the GMP Compliance Adviser. Click here for more information.

Username
Password
enlarge font size by using the short cut 'ctrl' and '+' (from IE 7, Firefox)