ADAMAS Consulting is delighted to announce the opening of our new office located in San Diego, California. ADAMAS brings 23 years of thought leadership in Quality Assurance to the American West.

The challenging year the industry has collectively faced has driven the ADAMAS team to stretch our imaginations. We have developed then implemented what the future of GxP, QA Training and Consulting, and indeed what remote auditing can achieve. Helping our clients overcome the most challenging QA barriers through data analytics, artificial intelligence, and big tech, while maintaining best in class privacy standards. Through our unique solutions, we are able to deliver our stringent quality standards globally, maintaining social distance, reducing our carbon footprint, all while keeping sensitive data safely locked away. And of course, we still pride ourselves on being the collaborative experts in what we do.

Our new location is in the nation’s hotbed of healthcare innovation and thought leadership. The ADAMAS team is continually inspired by the cutting-edge health care products our clients provide to people, and motivated to help our California based clients get lifesaving products to market faster and safer.

Please reach out to our San Diego based Business Development Manager, Marieke Gaudet Kirkman to talk QA programs, flexing with dynamic times, and ADAMAS new service offerings. We are looking to provide bespoke solutions to your most difficult challenges and are excited to connect with new California based clients.

If you would like to learn how ADAMAS utilise our extensive experience to ensure our clients needs are successfully met, please feel free to call us on  +1-919-341-3361 in the US; +44 (0)1344 751 210 in Europe, or email us at info@adamasconsulting.com.

The ADAMAS Team.

The ADAMAS Corporate Brochure 2016

 

Brochure – Please download the ADAMAS brochure describing our QA services and contact details.

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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.

 

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How to be a Clinical Auditor

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

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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.

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Is your QMS compliant?

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ICH (E6) R2 Addendum - Step 4

 

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How to be a Clinical Auditor

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


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