ADAMAS Consulting, a global leader in the provision of QA auditing and Quality Assurance services, will be attending this year’s virtual DIA 2020 Global Annual Meeting from June 14-18.

ADAMAS Consulting will be sharing our virtual exhibit page to share ideas and bring attendees up to speed with our own Quality Assurance innovations including our Remote Auditing services.

Come and e-Meet us.
Steve Bliss, Vice President, Business Development and Meredith Crute, Consultant will be hosting our exhibit page. Our team would love to discuss your challenging compliance and QA questions and how you are finding the current challenges facing the industry.

ADAMAS: Your trusted QA adviser
ADAMAS Consulting has been the leading provider of QA services and consulting for over 22 years and has conducted QA projects in 100 different countries for more than 750 clients. We provide 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 value-adding services, such as project benchmarking and Key Performance Indicator (KPI) tracking

We provide consistent quality in audit conduct and report deliverables, anywhere in the world. Whether it is GCP, GVP, CSC, GLP or GMP, ADAMAS has a solution that fits.

If you’re attending the DIA 2020 Virtual Global Annual Meeting, we look forward to connecting with you.
If you can’t make the event but would like to learn more about ADAMAS, please call us on +1-919-341-3361 in the US, +44 (0)1344 751 210 in Europe; or visit our website at www.adamasconsulting.com.

Hoping to connect online!
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?

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

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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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