A science and risk based approach to process validation
Differences between the process validation guidance from FDA (pharma), the draft from EMA (pharma) and the GHTF (medical device)
Practical quality risk management and its application
FDA process validation from design, process performance qualificiation to continued process verification
Continual improvement and process optimisation
The importance of a supporting Quality System
Past Events
Process Validation for Pharmaceuticals & Medical Devices in The EU & USA - Including Practical Workshop Exercises 2012 - 23-24 Oct 2012, The Rembrandt Hotel, London, United Kingdom (32171)
Important
Please, check "Process Validation for Pharmaceuticals & Medical Devices in The EU & USA - Including Practical Workshop Exercises" official website for possible changes, before making any traveling arrangements
