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Keep up-to-date with the latest news, events and industry insights.

Your Data is Safe With ADAMAS

Your Data is Safe With ADAMAS

Did you know that ADAMAS has made significant investment in compliance with international data privacy and security requirements, in ways that may not be reflected by other smaller organisations or freelancers? For example, all of ADAMAS’s activities are governed by a...

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KRIs and QTLs, Simplified

KRIs and QTLs, Simplified

It has been nearly four years since the release of ICH E6 (R2) in November 2016, however a recent poll on status of ICH E6 (R2) showed only 5% of companies as having implemented the addendum, with the top two hurdles being implementation of Risk Based Quality...

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Superior Vendor Compliance with ADAMAS

Superior Vendor Compliance with ADAMAS

Did you know that ADAMAS provides an enhanced level of compliance that you may not find when selecting other contract QA organisations or small/solo contractors? ADAMAS has made a significant investment in ‘state of the art’ compliance infrastructure and processes,...

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Second Wave, Second Strain

Second Wave, Second Strain

Could a second, potentially more contagious wave, of COVID-19 bring further disruption to travel and clinical trial activities? Is it possible to meet the current oversight and compliance expectations of regulatory authorities? We are all aware of the initial impact...

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Data Driven Quality Assurance

Data Driven Quality Assurance

“The only constant in life is change”-Heraclitus. This cannot be truer in today’s context. In the past two decades, clinical research industry, has gone through a paradigm shift from the use of paper-based systems to web based electronic systems and from traditional...

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21CFR11 Compliance of Third-Party Computer Systems

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ADAMAS Computer Systems Compliance (CSC)

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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

 

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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