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FDA's suggestions for changes to the cGMP regulations included among
others the call for a new chapter 'Process Validation'. For 'ensuring that
all necessary validation is carried out' (EU GMP Guide), many firms have
therefore introduced a position called validation manager. For this reason,
the ECA has established the certified Validation Manager Module. Attend a
compulsory course, "The Validation Manager", as well as two
further courses from our validation programme in order to obtain the
certificate for this high-level additional qualification.
 ECA will also recognise past ECA courses and conferences, e.g.:
- Computer Validation in GxP Compliance
- Lab Equipment Qualification
- GMP Compliance in QA Units
- Validation of Isolators
- Validation of Analytical Test Procedures
- Validation of Microbiological Test Procedures
The following link leads you to upcoming
events recognised for the
Certified
Validation Manager (ECA).
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