The Ministry of Health and Family Welfare, India, has granted approval to making the accreditation of Ethics Committees (ECs), involved in supervision of clinical trials, mandatory with effect from 01-Jan-18. The National Accreditation Board for Hospitals &...
ADAMAS is attending DIA Europe 2017 in Glasgow on March 29th-31st, stop by our exhibit stand (F18), meet two of our most experienced staff members, Carly Davenport, Business Development Director and Layal Lutfi, Executive Principle Consultant and Business Head MEA. If...
ADAMAS Consulting has been the leading provider of QA services and consulting for nearly 20 years…and counting. We’ve conducted QA projects in 90 different countries for more than 700 different clients. We’ve accomplished this by providing a unique QA outsourcing...
There are times in our professional lives when we are looking for a job change. When this search leads to ADAMAS, it may prompt the question, “Why is working at ADAMAS a good decision?” It might be beneficial to hear the perspective of a current employee, something...
We would like to thank you all for following our blog over the course of the last year and hope you will continue to do so in 2017. Please click the link below to see our Christmas Card. Click here to see the ADAMAS Christmas Card Hoping you all have a Merry Christmas...
“The RQA 2016 Annual Conference will be held at the Hilton Brighton Metropole 9-11 November 2016” Representing ADAMAS at this year’s RQA Conference will be Carly Davenport and Ian Brady, Heads of our Global CSV and GVP practices. Carly and Ian look forward to meeting...
ADAMAS Consulting (ADAMAS) is one of the world’s leading global providers of research Quality Assurance (QA) services offering auditing and consulting resources for all of the Good Practices (GxPs, where x is Clinical, Laboratory, Manufacturing, Distribution and...
ADAMAS was born (officially) on 1st September 1997, the year when the ‘new’ ICH GCP Guidelines were released – a happy coincidence in fact! Looking back, I can hardly believe we have been in business this long, and we’re still growing and expanding, which is the sign...
According to the Office Order dated 03-Jul-14 issued by the CDSCO, a Principal Investigator could not conduct more than three (03) clinical trials at any given period of time, irrespective of whether those clinical trials were actively recruiting or were in long term...
In Apr-13, the Medicines and Healthcare products Regulatory Agency (MHRA) successfully prosecuted an individual for manipulating pre-clinical analytical data. Following identification of irregularities in the bioanalytical data, the MHRA was notified and the following...
Come and meet ADAMAS Consulting at the RQA European QA Conference, Belfast
Computer Software Assurance (CSA): Why the Change and What Does it Mean?
Annex 1 Revisions: What are the Changes and Whom will they Affect?
Why Is Data Integrity Important When Transferring Data in a Clinical Trial?
ADAMAS and Ergomed combine to expand global capabilities