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, including secure user authentication, encryption of data in transit and at rest, robust backup and restore facilities, comprehensive Disaster Recovery and Business Continuity Plans, mobile device security management, logical data segregation, point of lowest permission and ‘zero trust’ access policies – as well as the suite of security measures that you would expect from anyone providing contract QA services, such as hardware firewalls, antivirus and antimalware protection and independent penetration testing. ADAMAS employees and subcontractors operate to stringent contractual requirements and, where applicable, Data Processing Agreements to ensure the highest levels of confidentiality and data privacy. There is a comprehensive Quality Management System in place, against which compliance is monitored, including policy level documents that address IT security and data privacy/protection. ADAMAS complies with GDPR and the UK Data Protection Act, as well as data privacy legislation in the territories in which we operate, and is registered with the UK Information Commissioner’s Office.

If you would like to discuss, please call us on +1-919-341-3361 in the US, +44 (0)1344 751 210 in Europe.

Ian Montague

Chief Executive Officer
ADAMAS Consulting
Ian.Montague@adamasconsulting.com

The ADAMAS Corporate Brochure 2016

 

Brochure – Please download the ADAMAS brochure describing our QA services and contact details.

×
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.

 

×
How to be a Clinical Auditor

So you want to be a Clinical Auditor? An article written by CEO.Dr.

×
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.

×

×
Is your QMS compliant?

Identify whether your QMS is compliant to the upcoming ICH GCP Addendum

×
ICH (E6) R2 Addendum - Step 4

 

Please enter your details to complete the download.

×

×
BECOME THE FIRST TO DISCOVER OUR DATA

Want to become one of the first businesses to access our exclusive data?
Get going and start reducing risk today. Pre register now.

×

×
How to be a Clinical Auditor

So you want to be a Clinical Auditor? An article written by CEO.Dr.


×

×