ProcedureCapture ensures that IT Systems and Applications in Regulated Industries are fit for purpose while also helping to produce the required documented evidence. 

Pharma and Life Sciences

Validation should be part of any development and manufacturing practice. It is also requested by 21 CFR Part 11(FDA) regulations and guidelines through the overall requirement that "equipment must be suitable for it's intended use".

Finance and

The Sarbanes-Oxley takes corporate governance, disclosure and financial accounting to new heights. The crux of the legislation - aimed squarely at public companies - centers on ensuring the accuracy, consistency, transparency, and timeliness of financial results and disclosures. 


The level of dependency on clinical decision support, and the growing requirements to meet with audit and overall risk-mitigation needs, continue to raise the bar for effective QA and patient-safety practices.  IT systems and applications therefore need to be fit for purpose and adher to regulatory standards such as DICOM, HIPPA and HL7. 

Oil and Gas

Constantly operating in highly vulnerable environments, Oil and Gas companies have to contend with a multitude of risks. To address these challenges, companies need to implement an integrated, risk-based approach to IT validation.

Food and Agri

IT systems are used in all segments of the food industry from growing, harvesting, processing, manufacturing, distributing, and merchandising to preparing food for consumption. Prerequisite programs such as current Good Manufacturing Practices (cGMPs) are an essential foundation.

ProcedureCapture® Overview

Short Online video which will give you a feel for the challenges and how ProcedureCapture solves these.

Validation Lifecycle flow with ProcedureCapture.

Find out why Customers and Partners think so highly of ProcedureCapture®

ProcedureCapture covers Requirements, Risk, Testing, Traceability and Defects with no add ons.

All from one integrated, affordable and easy to use tool.



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