[vc_row row_type=”row” use_row_as_full_screen_section=”no” type=”full_width” text_align=”left” background_animation=”none” css_animation=””][vc_column][vc_column_text css=”.vc_custom_1523969615206{padding-bottom: 40px !important;}”]Corrective and preventive actions are improvements to an organisation’s processes taken to eliminate causes of non-conformities or other undesirable situations. The CAPA module assists medical device companies to take control of incidents, deviations and corrective actions. Replacing a paper-based CAPA process with an electronic system and connecting it with change control, training and other quality systems can help assure the problem can never be experienced again.[/vc_column_text][vc_column_text css=”.vc_custom_1523890388148{padding-bottom: 30px !important;}”]
KEY BENEFITS
- Reduce risk of non-compliance
- Report and track quality events
- Trace issue root cause
[/vc_column_text][/vc_column][/vc_row]