At this year’s 2015 MAGI West Conference in San Diego, October 11th – 14th, ADAMAS Consulting will feature the industry’s only benchmarking service of QA audit findings that gives Sponsors the ability to better compare their audit results to industry averages.

For the past five years, ADAMAS has captured de-identified audit variables from the several hundred GCP and GVP audits that we have conducted – creating a database that provides live industry trends with regard to the frequency, criticality and specific observation types per audit on average.  ADAMAS now brings this performance management to your oversight activities with the ability to trend and report metrics on GCP and GVP audit findings

ADAMAS is an independent, global provider of QA and QMS consulting services across the entire GxP spectrum; providing services such as Investigator Site Audits, Vendor Systems Audits, PV, Laboratory and Manufacturing audits, as well as Mock Inspections, Inspection Readiness and GxP training to name a few.

We bring 18 years of experience as a company conducting clinical audits and QMS projects…serving more than 500 clients across 90 countries.

What distinguishes ADAMAS from all others is that we have a full-time, experienced staff of 28 auditors – including former MHRA (PV & GCP) inspectors – with offices in all three global regions (US, EMEA, and APAC) to support your global needs.  This allows ADAMAS to deliver high quality reports, with a consistency across all project deliverables.  We are, in fact, the global leaders in the delivery of EMA based PV audits.

Stop by our exhibit and engage with our team in person. Bring your compliance and QA challenges to our professional experts and auditors, and enter our raffle for your own personal Drone.

If you’re not attending the MAGI West Conference but would like to learn more about ADAMAS and our services, give us a call at +1-919-341-3361 or contact Steve Bliss at

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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