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

We have accomplished this by providing a unique QA outsourcing model to our clients:

• All our staff are full-time employed and trained to the highest standards
• For every project, we assign a dedicated Project Lead, providing one point of contact and clear project oversight
• We offer many value-adding services such as project Benchmarking and Key Performance Indicator tracking
• We can offer genuinely global coverage; whether it’s Buenos Aires or Mumbai, our staff deliver the same high standards

Awarded the “Best Poster” honors at this year’s 2017 SQA Annual Conference for the “Application of Audit Data and Metrics for Risk Mitigation and Effective CAPA”, ADAMAS is setting new standards for the industry in the collection, analysis and application of QA audit metrics.

Identifying critical risks based on actual data is key to conducting successful studies and meeting the requirements of ICH E6 (R2). ADAMAS believes that the QA function should be a major contributor to clinical operations in this process.

Come and meet the ADAMAS team at DIA (Exhibit booth #1352) and bring your most challenging compliance and QA questions to our professional experts and auditors. Donna McElcar, ADAMAS Vice President and Operations Head for the Americas Team, Ian Montague our COO, Carly Davenport, Business Development Director from our UK headquarters and Steve Bliss and Kirsten Kirkendall from the ADAMAS Americas group will all be there.

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

Hoping to see you in Chicago!

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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