Corrective and Preventive Actions (CAPA)

Automate the investigation of identified problems’ root causes, and corrective and preventative actions (CAPA) initiated by deviations, incidents, complaints, and other quality events to identify risks as a preventative measure against unwanted results, or their reoccurrence. 

Pre-configured workflow based on industry best practices

Integrated processes with deviation (non-conformance event).

Integrated investigation and assessments.

Tracking of execution and related change controls

Why Dot?

Effectiveness measurement

Full traceability and audit capabilities

Predefined KPIs and reports

User-friendly product

"  The product is user friendly. The flows in the system are the best practices that are used in the pharmaceutical industry (21 CFR Part 11, Annex 11, GAMP 5). Almost no adjustments (customizations) are needed. The validation package is very thorough and comprehensive. The software is stable almost without faults."

Computerized Systems Validation in Pharmaceutical 

Bella B.

 Good value for money

"    The overall experience is good, the company uses the system as part of our routine and it has become part of our DNA. we get good support when needed, numerous aspects of the QMS are captured in one system - easiness of use - easy communication with other company employees "

Yoel B.

Avoid lengthy design and configuration processes with our core QMS processes

Dot Compliance is the leading 

ready-to-use Quality Management Software

Start streamlining CAPA management in a matter of days

A simple, powerful and affordable way to manage your quality processes.