ADAMAS is attending DIA Europe 2017 in Glasgow on March 29th-31st, stop by our exhibit stand (F18), meet two of our most experienced staff members, Carly Davenport, Business Development Director and Layal Lutfi, Executive Principle Consultant and Business Head MEA.

If you are attending DIA Europe 2017, we look forward to meeting you. Bring your most challenging compliance and QA questions to our professional experts and auditors, and enter our free raffle for Amazon Gift Vouchers.

ADAMAS Consulting has been the leading provider of QA services and consulting for nearly 20 years…and counting. We’ve conducted QA projects in 90 different countries for more than 700 different clients.

If you are not attending but would like to learn more about ADAMAS, please call us at +44(0)1344 751 210 in Europe; +1-919-341-3361 in the US; or visit our website at to leave us a note.

Hoping to see you there!

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


Please enter your details to complete the download.



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