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Clarmon guides companies in developing and implementing GMP compliance strategies, assisting them with FDA pre- and post-approval inspections, QA/QC documentation review, regulatory interpretation and submissions.

As appropriate and according to client needs, we perform internal audits and general GMP compliance auditing. Audits are tailored to meet the specific requirements of your company, and help achieve compliance with regulatory requirements in the most efficient way appropriate.

Clarmon can also assist your company in the development of GMP Quality Systems.

We also provide consultancy in:



Clarmon provides you with a range of solutions to plan, implement and operate your compliance management system in a cost-effective manner.


Our consulting service will assess your needs rapidly and design a solution within an agreed time and cost framework.


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Designed by experts in FDA and GxP regulations, Clarmon's training programmes...

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It is Clarmon policy to commit to customer satisfaction and to provide....

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We deliver the software - along with the engineers and consultants...