Hi everyone, we hope you are all looking forward to the 1st European QA conference in Bonn, next week, as much as we are.

The conference will be a great opportunity for the European Quality Assurance community. It is an exciting prospect to finally meet and share ideas with QA colleagues, throughout Europe.

We are particularly looking forward to hearing the keynote speaker, Manfred Müller’s different perspective that he can add through his experience both working in and lecturing on risk management. His ideas on quality assurance through group quality control to reduce the chance of human error are particularly pertinent to the Pharmaceutical industry.

We are eagerly anticipating meeting you at the conference at the Maritim Hotel. Please feel free to come down and talk to us about our services and how ADAMAS may be able to help. Along with our European representatives being in attendance our heads of business from India and the United States will be visiting. They will be more than happy to talk about differences between working in Europe and their own markets with you and the knowledge that can be shared across them.

When you come and see us at Stand #6 there will be the opportunity to win an excellent Google Nexus 7 for the small price of your business card.

Visit our conference specific webpage http://adamasconsulting.com/news-eu.asp to find out more details about our company and the services we can provide to you.


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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