|
Title |
Level |
Summary |
Length of Seminar |
|
Auditing for GMP |
Advanced |
Auditing practice both from point of view of the
auditor and the auditee |
2-3 days in English
4-5 days in 2 languages |
|
Risk Management |
Advanced |
An introduction to risk management in the context
of pharmaceutical manufacturing |
2 days in English
4 days in 2 languages |
|
Cleaning Validation |
Advanced |
An overview of cleaning validation including case
studies |
2 days in English
4 days in 2 languages |
|
Change Control
New |
Advanced |
External and internal requirements for change
control within pharmaceutical manufacturing |
1-2 days in English
3-4 days in 2 languages |
|
Root Cause Analysis
New |
Advanced |
How to conduct investigations of discrepancies,
complaints and out-of-specification results using a range of tools and techniques |
1-2 days in English
3-4 days in 2 languages |
|
An overview of GMP
New |
Basic(Suitable for non-manufacturing personnel
who need a basic understanding of GMP) |
An introduction to GMP requirements, using a case
study in which syndicates design and build their own product and company systems |
2 days in English
4 days in 2 languages |
