Come and meet the ADAMAS Americas team!

At this year’s Society of Quality Assurance (SQA) 2016 Annual Meeting in Grapevine, Texas, Donna McElcar, Vice President at ADAMAS Consulting LLC, has been selected by the SQA to co-chair and co-present the Quality College sessions “Problem Definition – Moving Beyond Human Error” and “CAPA Creation and Effectiveness – Beyond Training”.

During the annual meeting, our ADAMAS team will also be delivering 3 poster presentations including:

  • Investigator Oversight-Five Chronic Audit Observations
  • Conducting Remote Vendor Audits
  • Patient-Friendly Informed Consent

The ADAMAS Americas team is part of a global group of full-time, experienced GxP Auditing, QA and QMS auditors and consultants that also includes former MHRA GCP and GVP Inspectors and staff based from Mumbai to Buenos Aires. So no matter how many audits or geographies your audits span or which GxP ADAMAS provides an unparalleled consistency and quality across all of our audits and projects…which means more time for you to focus on your other priorities.

If you’re attending the conference in Texas, stop by Booth #302 and meet the ADAMAS Americas team in person. Bring your compliance and QA challenges to our professional experts and auditors, and enter our raffle for your own drone.

If you’re not attending but would like to learn more about ADAMAS, give us a call at +1-919-341-3361 or visit our website at www.adamasconsulting.com or contact Steve Bliss at steve.bliss@adamasconsulting.com

See you there.

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. Patricia Fitzgerald.

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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?

 

Is your QMS compliant to the upcoming ICH E6 Addendum? Download our 5-point checklist

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ICH (E6) R2 Addendum - Step 4

 

Please enter your details to complete the download.

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