Blog

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

Paediatric Clinical Trials

Although medicinal products for use in adults undergo extensive pharmacological, stability and toxicological testing through clinical trials, this same approach has not always been applied to medicinal products to treat children.  As a result, many products are used...

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QA as a Service

As a service company we keep in mind the old adage that ‘the customer is always right’.  But is this really appropriate in QA?  I guess you would say it depends on who the customer is. In our business, the customer is the company/person that commissioned the...

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Medical Devices

ADAMAS recently held an internal training session for all their consultants on the topic of Investigational Medical Devices (IMDs).  This was run Dr Joerg Holzinger, ADAMAS’ ‘subject matter expert’ in response to an increasing number of enquiries for assistance in...

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Trial Master File Reference Model

The Trial Master File (TMF) comprises all those essential documents which individually and collectively permit evaluation of the conduct of a trial and the quality of the data produced.  These documents serve to demonstrate the compliance of the investigator, sponsor...

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Archives

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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