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...
ADAMAS
ADAMAS Consulting is delighted to announce the opening of our new office located in San Diego, California
ADAMAS Consulting is delighted to announce the opening of our new office located in San Diego, California. ADAMAS brings 23 years of thought leadership in Quality Assurance to the American West. The challenging year the industry has collectively faced has driven the...
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...
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,...
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...
Do you protect your staff or your Clinical Trial?
It’s a tough choice – new drugs for patients or the health and safety of your valued staff? With ADAMAS Consulting, you do not have to choose. As we keep hearing these are unprecedented times, and just recently there have been concerning articles in the scientific...
FDA Announces the Retirement of the MedWatch to Manufacturers Program
The U.S. Food and Drug Administration has announced the retirement of the MedWatch to Manufacturer Program (MMP) as of 31st July 2020. The program provided participating drug and biologic manufacturers with a means of receiving information from the FDA on serious...
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...
ADAMAS Consulting is set to bring Quality Assurance innovation and collaboration to the DIA 2020 Virtual Global Annual Meeting
ADAMAS Consulting, a global leader in the provision of QA auditing and Quality Assurance services, will be attending this year’s virtual DIA 2020 Global Annual Meeting from June 14-18. ADAMAS Consulting will be sharing our virtual exhibit page to share ideas and bring...
Annual MHRA GPvP Inspection Metrics Report – Apr 2018 to Mar 2019
The Medicines and Healthcare products Regulatory Agency (MHRA) recently published their latest Good Pharmacovigilance Practice (GPvP) inspection metrics covering the period April 2018 to March 2019. Within this period a total of 18 inspections of Marketing...