In today’s highly regulated pharma, device, and veterinary industries, it is essential to use the most efficient processes and ensure compliance with corrective and preventative action (CAPA). Regulatory inspectors are increasing reviewing responses to findings dealt with by the CAPA approach and process improvement. It is highly likely that the organsations who have been inspected will be assessed at next inspection in terms of whether the corrective and preventative actions have been implemented -- has the organization done what it said it would? If previous major findings have not been addressed then a critical finding may be given. This course is ideal for learning how to improve industry procedures and processes, and implement and document an effective CAPA quality system.
Improving Processes & CAPA
Apr 14th, 2008
London, --
GB
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