ADAMAS Consulting has been the leading provider of QA services and consulting for 20 years and has conducted QA projects in 100 different countries for more than 750 clients. 

We have accomplished this by providing a unique QA outsourcing model to our clients: 

  • Our staff are all full-time employees and trained to the highest standards 
  • For every project, we assign a dedicated Project Lead, providing one point of contact and clear project oversight 
  • We offer many value-adding services such as project Benchmarking and Key Performance Indicator tracking 

This means that we deliver gold standard services on time, every time.  

We offer unparalleled quality, in audit conduct and report deliverables, consistently, anywhere in the world; whether it is GCP, GVP, CSC, GLP or GMP ADAMAS have a solution that fits, delivered by our dedicated, highly experienced, highly trained and motivated team.  

At ADAMAS we pride ourselves on being great to work with. 

All this translates into more time for our clients. 

ADAMAS will be attending this year’s Drug Information Associations (DIA) European 2018 Conference in Basel, Switzerland from April 17th19th. Carly Davenport, Business Development Director, and Angela McCullagh, Director, Operations EMEA will be at our exhibit (booth 102) to meet with you.  

If you are attending DIA 2018, we look forward to meeting you. Bring your most challenging compliance and QA questions to our professional experts and auditors and enter our prize draw to win a Belkin Wireless Charger. 

If you are not attending but would like to learn more about ADAMAS, please call us at  +44(0)1344 751 210 in Europe; +1-919-341-3361 in the US; or visit our website at  to leave us a note. 

 

Hoping to see you there! 

The ADAMAS Team 

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-quality-assurance-services

 

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.

×
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?

Identify whether your QMS is compliant to the upcoming ICH GCP Addendum

×
ICH (E6) R2 Addendum - Step 4

 

Please enter your details to complete the download.

×

×
BECOME THE FIRST TO DISCOVER OUR DATA

Want to become one of the first businesses to access our exclusive data?
Get going and start reducing risk today. Pre register now.


×

×
How to be a Clinical Auditor

So you want to be a Clinical Auditor? An article written by CEO.Dr.


×
How to be a Clinical Auditor

×
How to be a Clinical Auditor

×