blog-image-lg-posterDana Beck, one of our leading Consultants for ADAMAS Consulting in the Americas, was recently honoured by the Society of Quality Assurance and awarded the “Best Poster” accolade at the SQA 2015 Annual Conference held in Tampa, Florida the week of April 12th.

Her Poster, ”Be Forewarned! Inform with Caution! Are we enlightening or overwhelming potential subjects?” reflects Dana’s insights and passions for the continuous improvement of the Informed Consent process.

Ms. Beck was inspired to investigate the best tools for the informed consent form and process through her years as a clinical auditor.  She also happens to be married to a wonderful 8th grade history teacher who provides direct feedback from people with that educational level.  Through her research she was able to suggest additional age, socio-economic, and comprehension targeted strategies that should be deployed during the informed consent process rather than relying on a dozen or more written pages.

ADAMAS is tremendously proud of her dedicated work and commitment to better research practices.

It is truly an honour to be recognized as such by one’s peers.

As a leading provider of clinical audits and Quality Assurance Consulting services on a global basis, ADAMAS continues to be a leading contributor to the advancement and thought leadership driving our industry.

If you would like to speak with any of our experts, including former FDA and MHRA Inspectors, or to learn more about ADAMAS, 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


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Is your QMS compliant?


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ICH (E6) R2 Addendum - Step 4


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