We’re proud to announce that Mr. Daniel Vazquez has joined ESTERN Medical CRO Life Sciences as the Head of Clinical Trials Regulatory Advisory Board.
Within the past years, up to 78% of FDA-regulated clinical trials for the top pharmaceutical & medical device companies are conducted outside the U.S.
The ESTERN Medical CRO Life Sciences & Consulting Group, a life science clinical trials, regulatory, quality and clinical consulting firm, recently announced the launch of its clinical R&D Articles Series, an interactive knowledge of publications articles circuit featuring ESTERN most experienced clinical scientific strategic thinkers.
In the past 15 months, since the World Health Organization declared Covid-19 as a pandemic, healthcare systems around the globe have been under immense clinical trials R&D and regulatory pressure.
The United States has what is arguably the most complex healthcare system in the world. As a result, changes within the industry are slow. To understand what may come, it helps to have a deeper understanding of healthcare’s complexity.
The challenges from the impact of COVID-19 in the Clinical Research has pivot into decentralized (virtual) Clinical Research trials.
During the past year 2020 and present 2021 our company has engaged in diverse solutions to catalyzed or accelerate processes in diverse angles in this global pandemic, internally and externally, to our Life Sciences clients.