Biobanking Clinical Research Research Trials 
AuroBlog - Aurous Healthcare Clinical Trials blog
FEBRUARY 13, 2024
The analysis included health information from 273,260 female participants in the United Kingdom Biobank, and the findings suggest that those who start their period younger and go […]
pharmaphorum
JANUARY 18, 2023
Pharmaceutical companies and biotechs are also adapting their approaches, launching patient finding and engagement programmes that can start years before clinical trials begin and allow them to run ‘recontact by genotype’ studies that the Resilience Project would have liked to do. Why should research be any different?
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Crucial Data Soutions
JUNE 28, 2021
It’s 2021 and sharpies are still being used to write on bio sample tubes in most clinical trials…. As most people would agree, one core tenant of a well-run clinical trial is accurately collecting, handling and analyzing bio samples from subjects during the study. Background.
The Pharma Data
AUGUST 30, 2021
Borja Ibáñez, group leader of the Translational Laboratory for Cardiovascular Imaging and Therapy at the CNIC, cardiologist at the Hospital Universitario Fundación Jiménez Díaz (FJD) in Madird, and member of the CIBERCV cardiovascular research network. The study is a prime example of collaboration between basic and clinical researchers.
XTalks
FEBRUARY 4, 2021
Data generated through high-throughput omics approaches paired with clinical patient records can give rise to remarkably robust datasets to inform and guide disease insights and development of targeted therapeutics. Generation of strong research dataset cohorts must begin with high-quality clinical samples.
The Pharma Data
JANUARY 31, 2021
The need for sharing information across the medical research landscape was never starker than during the early days of the COVID-19 pandemic. According to Nature Biotechnology, “81% of researchers are constrained by the inadequate quantity and quality of biospecimens and 80% of companies find accessing materials difficult.”.
Advarra
FEBRUARY 13, 2024
Every day, clinical research organizations work to deliver a seamless user experience for their staff, while also providing robust security measurements to protect their data and stay compliant. Having a singular password could also potentially affect trial timelines.
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