ADAMAS consultants have the necessary depth of knowledge and experience to identify the compliance failures that have the biggest impact on your organisation. We apply critical thinking to solving compliance issues as pragmatically and efficiently as possible.

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Vision, Experience, Understanding

ADAMAS has the vision, experience and understanding of our clients’ needs to assist them in meeting their business goals. We recruit, train and develop high-calibre professionals, and we are committed to the highest standards of excellence, integrity and performance.

Find out how ADAMAS Consulting can help with your next project

Our Global Reach

ADAMAS has conducted thousands of GxP audits in more than 85 countries for over 500 international clients, and we are committed to providing all our clients with the highest level of service in every country.

With offices in three continents, our global capabilities allow ADAMAS to provide coverage for a wide range of healthcare clients, operating internationally. Our personnel are comprised of highly skilled, experienced professionals, and we pride ourselves on the longstanding relationships that we have developed with major healthcare companies.

Our People

ADAMAS has a growing team of full-time, employed permanent consultants based in three regional offices. The average QA experience of the team is over 10 years, with most of them having many years experience in operational roles before transferring to QA, namely Clinical Development, Pharmacovigilance, Data Management, IT and Regulatory Inspections.

Our experienced consultants are specialists in GCP, GVP, GLP and GMP QA and can provide all of your auditing and quality consulting needs across the product development process from toxicology to pharmacovigilance.

Download Our Brochure

Find out more about ADAMAS and our global QA services. Also featured is our GCP and GVP Audit benchmarking data.

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I trust the ADAMAS team’s work as much as I do their total professionalism. ADAMAS is a pleasure to work with.


Regulatory Compliance Manager, Biotech Company

Contact Us

If you've got any questions or queries about our services, careers, or training, please get in touch.
We have 500+ years combined experience, working around the globe there isn’t anything we’ve not encountered in our sector. We're very approachable and happy to help.

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The ADAMAS Corporate Brochure 2016


Brochure – Please download the ADAMAS brochure describing our QA services and contact details.

Regulatory Environment


The development of medicines is the most regulated industry in the world, and compliance at each stage of the research and development process, as well as after licensing, is critical to ensuring high quality and safe medicines reach patients in a timely manner.



ADAMAS’s consultants have expertise across the G’X’Ps in pre-clinical, clinical and post-licensing areas. They have worked across many different therapeutic areas and product types including oncology, vaccines, biologics, medical devices and gene therapy. As a company we have developed close partnerships with our clients to support them in their development programmes and post-licensing activities, and to guide them successfully through their worldwide regulatory inspections.


How to be a Clinical Auditor


‘So you want to be a Clinical Auditor?’, an article written by CEO Dr. Patricia Fitzgerald.

Benchmarking Data


Please download our benchmarking data sheet, to see how these data compare with your own performance. To discuss a more detailed report, or analysis of a data subset, please get in touch.

Is your QMS compliant?


Is your QMS compliant to the upcoming ICH E6 Addendum? Download our 5-point checklist

ICH (E6) R2 Addendum - Step 4


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