With FDA's new Process Validation Guidance validation requirements will become more complex. In addition to other requirements the revised Annex 15 also asks for a Process Validation Life Cycle. For 'ensuring that all necessary validation is carried out' (EU GMP Guide), many firms have 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 to obtain the certificate for this high-level additional qualification.
For questions relative to the ECA Certified Validation
Manager, please contact
To receive the certificate, the applicant must attend three
out of the following courses / conferences. After attending
the third course, the applicant obtains the certificate "ECA
Certified Validation Manager".
- Cleaning Validation
- SPC in the Pharmaceutical Industry
- The Validation Manager
- Continued/Ongoing Process Verification – how to handle part 3 of the validation life cycle
- Process Validation in the light of the Annex 15 and FDA requirements
>>> LIST OF ALL COURSES AND CONFERENCES CURRENTLY OFFERED AND ACKNOWLEDGED IN THIS PROGRAMME (including detailed information on every event – venue, dates, fees and agenda as PDF; just click on any event in the list)