as of 2019 - 07 - 01

21.B Regulatory principles

21.B Regulatory principles
Here you will find answers to the following questions:

What general GMP rules are there for manufacturing active substances?

What additional factors must be considered for biotechnological active substances?

Is an authorisation from the competent authority required in order to manufacture and import active substances?

What has to be considered in importing active substances?

How are active substances released?

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)