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.

We’ve 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

The resulting benefit is that we deliver gold standard services on time, every time. We offer an unparalleled level of quality of “in audit conduct” and report deliverables, consistently, anywhere in the world; through the efforts of our dedicated, highly experienced, highly trained and motivated team. All this makes working with ADAMAS easy.

This translates into more time for our clients to focus on all other priorities.

ADAMAS will be attending this year’s Society of Quality Assurance (SQA) 2017 33rd Annual Meeting in Maryland from March 26th-31st. Donna McElcar, ADAMAS Vice President and Operations Head for the Americas Team, will be at our exhibit (booth 103) to meet with you. Donna has also been selected by the SQA to lead the Quality College sessions “Problem Definition – Beyond Human Error” and “CAPA Creation and Effectiveness – Beyond Training”.

If you are attending SQA 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 an Amazon Echo.

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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