4th Global QA Conference & 30th SQA Annual Meeting

The 30th Annual Meeting and 4th Global QA Conference will be held Tuesday – Thursday, 8th – 10th of April 2014. Three days of plenary and concurrent sessions will explore hot topics and the latest regulatory interpretations in the field. Sessions will focus on regulatory-based topics in manufacturing (GMPs), preclinical (GLPs) and clinical (GCPs) research arenas.

ADAMAS Consulting will be exhibiting at the event in Las Vegas from 8th – 10th of April.

Come and meet ADAMAS Directors and Consultants on stand #100 to talk about Services & Solutions we can provide to benefit your business. Plus a chance to Win a Kindle Fire tablet!

For more information on ADAMAS at this event – click here

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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