ADAMAS was born (officially) on 1st September 1997, the year when the ‘new’ ICH GCP Guidelines were released – a happy coincidence in fact! Looking back, I can hardly believe we have been in business this long, and we’re still growing and expanding, which is the sign of a healthy company 

We are a very different company to when we first started in 1997 with only five of us. Today we have 37 permanent staff, and have just recruited three more consultants, with plans to recruit a further three in the next year.

Our vision has never changed in all those years – we aim to be the #1 choice for research quality assurance, and we do this by hiring the best people with deep industry experience and knowledge to deliver exceptional client services.

Patricia Fitzgerald

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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