With 56% of the world’s population residing in Asia, it is an attractive destination for clinical trials.   However, maintaining the quality and integrity of the clinical research data in the emerging markets has always been a challenge for the pharmaceutical, biotechnology and medical device companies.

ADAMAS with its rich pool of experienced auditors located regionally extends it’s capability with a new Asia & Pacific office in Mumbai helping you address your quality management challenges in the fields of GCP, GLP, GPvP, GMP and Computer Systems Validations.

Collectively ADAMAS Consulting has worked with over 200 international clients in more than 60 countries worldwide and has offices located strategically in the UK, USA, Germany and now India. Bringing you global expertise with local knowledge and understanding.

ADAMAS Consulting, UK has opened its wholly owned subsidiary ‘ADAMAS Clinical Quality Consulting Private Limited (ADAMAS Pvt)’ in Mumbai to meet the growing demands of quality assurance in the Asia Pacific region.

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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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