Welcome to the brand new Adamas Consulting CQA blog on the brand new website. With the launch of the new site, we’ll be launching few new features; a blog where we’ll be talking about the latest news and events from Pharmaceutical & Biotech industry; Linked in and Twitter direct links for the newest information and updates on Adamas and You Tube channel to have an inside look on Adamas.

We are so excited with the launch of Adamas new website just in time for Easter!

On our Linked in group’s page we’ll be open to answering your questions and addressing topics!

You never know, we just might answer your questions right here! Please subscribe to this blog where you can also write your comments about the articles, or follow us on twitter or Linked in for quick updates.

Adamas Consulting is an international consultancy providing a full range of independent GCP, GLP and GMP Clinical Quality Assurance ( CQA ) audits and GPVP services. We have offices in UK, Germany and USA from which we conduct clinical audits all over the world.

ADAMAS Consulting also provides a comprehensive Computer System Validation (CSV) audit service in all stages of the life cycle of a computerised system.

Let us know what you think.

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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