Free EDC Software for Non-Profit COVID-19 Related Studies
Call To Pool Research Resources into Large Trials to Generate Evidence On COVID-19 Treatments
Offer for Trial Planning Software for COVID-19 Sponsors
FDA Issues Guidance for Conducting Clinical Trials During COVID-19
Latest in People and Business News
The latest happenings in the industry from the past month, all in one place.
ClinCapture to Provide Free EDC for Researchers Investigating COVID-19 Treatment
COVID-19 Upends Business-as-usual Research and Regulatory Practices
Now officially a worldwide pandemic, the biomedical research community is rushing to develop treatments and preventives to halt the spread and severity of the COVID-19 virus.
The Challenges of Developing CAR-T and cas9 Therapies
Jing Zhao, Chief Business Officer of Refuge Biotechnologies, discusses how dead cas9 can be leveraged to completely control gene expression without making permanent edits as seen with CRISPR technology.
Advancing Human Healthcare Through Accessible Trial Data and Analytics
The Clinical Study Data Request consortium is actively pursuing platform interoperability to allow data to be merged and analyzed as an important step for advancing human healthcare.
Illingworth Research Launches PatientGO
Medable Releases Global TeleVisit Capabilities
Investing in Data Science to Unlock Clinical Data Value
The need for biopharma companies to equip data managers with the training and resources necessary to capitalize on new digital health tools.
Clinical Data Manager: A Roadmap for the Future
Breaking down the evolving role of today’s clinical data manager-and its importance as a key cog in the clinical research ecosystem of tomorrow.
How Patients Can Leverage AI to Find the Right Clinical Trial
Tzvia Bader, CEO of TrialJectory, discusses how the company’s AI-powered technology platform is democratizing cancer care and expanding access to advanced new treatments.
Clinical Trials Feel the Coronavirus Crunch
With the Coronavirus causing significant disruptions in the clinical trials industry, Sponsors should expect data quality issues due to missed visits and a reduction in enrollment rates.
Post-Brexit Britain Aims to Match EU Rules on Trial Authorizations
Though on its way out of the European Union, the UK is trying to align its trial approval practice with the EU’s new clinical trial regulation.
Overcoming Observation Clinical Study (Patient Registry) Development Challenges
Ravi Jandhyala, Consultant Pharmaceutical Physician at Medialis and an expert in rare disease patient registries, discusses how to overcome clinical trial registry challenges.
Why You Should Expand Your Patient Advocacy Strategy to Include Health Influencers
With radio, billboard, TV, and digital advertisements being left in the dust, additional engagement from influencer communities are more likely to be reach patients.
Pivotal Acquires Akcelis
Novotech Wins Contract for Komipharm Coronavirus Covid-19 Trial in South Korea
What You Need to Know About Adaptive Platform Trial Design
Allyson Gage, Chief Medical Officer at Cohen Veterans Bioscience talks about her perspectives on platform trial design.
Medidata and Medpace Sign Agreement to Integrate Data into Platform
Merz Pharma’s RBQM Journey
A case study of the risk-based quality management learning curve.
WCG CenterWatch iConnect Selected for The Michael J. Fox Foundation’s Fox Trial Finder
