This week, ADAMAS consultants are conducting audits for a variety of clients around the world in Israel, Saudi Arabia, Dubai, India, Germany, Poland , USA, United Kingdom, Italy and Canada.

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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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

 

Please enter your details to complete the download.

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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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How to be a Clinical Auditor

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How to be a Clinical Auditor

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