Process Validation

Process Validation

Course Content: 

Be familiar with the definitions and terminology of validation. Know about the lifecycle of validation. Appreciate the quality regulations pertaining to the Medical Device industry. Be familiar with the documents containing quality regulations. Consider what happens if validation goes wrong. Appreciate their own role in the product they validate, make or support. Understand the role of process control in maintaining a validated state. Consider the difference between validation and verification. Appreciate the documents and records required to support process validation. Understand basic concepts of supporting regulations such as Part 11 compliance.

Learning Outcomes: 
Understand the context of Process Validation within the Quality Management System
Name of Trainer: 
Pacina Ltd
Course Venue: 
Charleville Park Hotel
This is a foundation course in Process Validation for medical technology industry.
Start Date: 
27th September 2017
Course Days and Times: 
1 Day 27 Sept 2017
Subsidised Fee for Network Member Company (€): 
Course Fee for Non-member Company (€): 

Register Your Interest

Please read the Eligibility Criteria.

This form expresses your interest in this training course. 

This question is used to help prevent automated spam submissions.

Any Questions? Contact us

Michelle Reinecke Quain


Enterprise Led Learning and Training Networks

5th Floor, Q House, 76 Furze Road, Sandyford, Dublin 18, Ireland.

+353 1 2079630