Everything you need to become “Audit Ready”

AuditMan is the ultimate QMS Platform for internal and external audits, supplier audits, CAPA and complaint management, change control, feedback, and documents control for Medical Device companies.

While being fully scalable to your company size, AuditMan is designed with small-medium medical companies in mind, who would like to have a centralised electronic solution for their QMS.

AuditMan improves your quality system workflows, reduces costs associated with nonconformances (both raised internally and externally by auditing organisations), and ensures that findings are resolved and closed in an efficient way. AuditMan does NOT give you ‘bells and whistles’; it gives you only all what is necessary for an effective QMS.



Companies can raise and manage supplier CAPAs, and Supplier Audits via the AuditMan platform.


All QMS documents and records can be uploaded on AuditMan for access by all internal staff and auditors, while ensuring security of data.


AuditMan is loved by consultants and 3rd party internal auditors who manage internal audits of several clients in a single platform.

External Auditors

Regulatory auditors use AuditMan as it streamlines evidence requests, and ensures effective follow up of audit trails until closure.


Employees involved in audits know exactly what is needed from them, when it is needed, and who needs it. This ensures seamless process in place.


Import audit checklists for your auditors to follow and ensure compliant coverage and consistency. AuditAct provides the most comprehensive audit checklists that are also used by our own auditors and consultants.

Driven by Real Industry Needs


AuditMan is not only based on what is needed now; we have identified the needs your future organisation and the regulatory environments


We only do what we do best. We only support medical device and healthcare industry.



AuditMan is made after full review and use of all key quality management systems out there. AuditMan has identified, and addressed the gaps and built on top of them.


AuditMan is made with two things in mind; to meet our client’s requirements, and compliance with their regulatory requirements.

Standards and Regulations

AuditMan is specifically designed for medical device companies who run or plan to run a ISO 13485, CE, or MDSAP and 21 CFR 820 compliant quality management system. No one-size-fits-all approach; we only work in our area of expertise – our “ikigai”, that’s medical devices.

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