“The RQA 2016 Annual Conference will be held at the Hilton Brighton Metropole 9-11 November 2016”

Representing ADAMAS at this year’s RQA Conference will be Carly Davenport and Ian Brady, Heads of our Global CSV and GVP practices.

Carly and Ian look forward to meeting you at the conference and are ready  to discuss your local and worldwide Quality needs covering all the GxPs and including Investigator Site Audits, Vendor Systems Audits, Pharmacovigilance, Laboratory and Manufacturing audits, as well as specialized services for Mock Inspections and Inspection Readiness.

With nearly 20 years as the leading independent provider of Quality Assurance services, ADAMAS has exceeded our clients’ primary demands for the delivery of high quality auditing services and reports, consistently, across all audits and projects no matter where they are conducted in the world. We accomplish this with our unique business model that supports a global team of fully employed, ADAMAS auditors and consultants…unlike other service providers that rely on independent contractors and freelancers. Our dedicated staff of full-time consultants spans the globe, with our most recent addition based in South America

We can bring local regulatory expertise to your global QA activities.

Our GVP practice was set up two years ago as a response to the introduction of new regulations. GVP has become ADAMAS’ fastest growing service offering. Ian Brady would be delighted to talk to you and highlight the services we can offer in areas such as:

  • Global Headquarters (HQ)
  • Local Company Affiliate
  • Marketing Partner
  • Distribution Partner
  • CRO/Vendor/Service Provider (Individual Case Processing/Literature Search)

So stop by our Stand #7, meet our team, share insights, and enter our prize draw to win an amazing Amazon Echo. If you’re not attending but would like to learn more about ADAMAS’s services, give us a call at 01344 751210 or contact Carly Davenport at  carly.davenport@adamasconsulting.com

Come and meet us! We look forward to seeing 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


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