The g-CAPA™ module is based on the principle
of ‘continuous validation’. The process allows collection of
customer complaints, observations, audit findings, adverse effects
and QA data.
Any of these ‘Initiation’ events follows a defined process
to a ‘Close Out’ event which can include SOP change, equipment
modification, re-training and re-validation.
Your existing CAPA process can be simply configured into a secure, auditable and collaborative environment that allows you to control, monitor and report on your CAPA process.
CAPA forms are stored on g-docs™ and can easily integrate with the SOPs module, g-train™ (or your own in-house LMS), and ValMan™ or your validation management software. Forms can be signed in the digital environment using CoSign® or your digital signatures package.
For more information contact CAPA@goodproductsEU.com