There are many important tasks and activities required to set up and successfully run a clinical trial. More than ever, clinical sponsors and CROs are
In recent years, the use of artificial intelligence (AI) in the healthcare industry has been rapidly growing, with applications ranging from medical imaging analysis to
Scientific research for bright future world Lorem ipsum dolor sit amet, consetetur sadipscing elitr, sed diam nonumy eirmod tempor Discover More 0 + Years of
The COVID-19 pandemic changed the way that we people live and work. Everything went online, from ordering groceries to remote collaboration with coworkers. The vaccines
With numerous eTMF software options available in the market, it is essential to know what features to look for when selecting the right solution for your clinical trials.
Learn how seasoned experts evaluate and successfully select CRO Partners
SureClinical eTMF Passes FDA Inspection Clinical trial systems and processes are advancing at a fast rate. We’ve come a long way from truckloads of paper
Clinical operations ecosystem for Clinical Research Organizations streamlines and accelerates the delivery of new treatments to patients globally RENO, NV – December 16, 2021 –
The challenges facing clinical trial teams today Life Science Clinical Operations teams struggle to connect, collect, access, view, report, analyze, and understand data from
Every day, individuals are more and more likely to sign documents electronically. But, just what is an electronic signature? Are there different types of signatures?
Clinical trials are incredibly important for bringing safe and effective treatments to market to help patients who need them. With that in mind, the International
Clinical trials continue to be burdened with paper and manual processes. Sometimes hybrid situations are used where there are some paper processes and some manual
By Guest Author: Dr. Karin Köhler-Hansner As a sponsor, do you contract out your clinical trials to a CRO and forget about them? Do you
The COVID-19 pandemic has affected how we run clinical trials, and those Sponsors, CRO’s and Sites that are able to manage trial and patient data
If you are like many organizations who have implemented or considering a work-from-home policy for the immediate term or planning a broader long-term strategy with
Trust is the cornerstone of all health and life science interactions, whether it’s following Good Clinical Practice in running clinical trials or in a patient-doctor
Implementation of an advanced CTMS, eTMF and eClinical platform can bring huge benefits to a business. The FDA has adopted digital submission requirements and the
The pursuit of optimizing the clinical trial process frequently relies on the intense effort to manage the trial project with a clinical trial management system
Whether you’re a CRO being constantly audited by your Sponsor, or part of a pharmaceutical company preparing for your first FDA Pre-Approval Inspection (PAI), in
This is the first in a series of blog posts sharing the expertise and voices of SureClinical employees, advisors and customers. This blog is focused on
SureClinical Announces SureCTMS, First Mobile eClinical Trial Management System SureCTMS™ delivers the first clinical trial management system with an easy-to-use, mobile-first design for web, Apple
Like a LinkedIn™ for the health sciences market, SureNetwork will lower clinician recruitment and staffing costs through a collaborative network of trusted health science organizations
Forward-thinking Biopharma and healthcare companies are increasingly looking to cloud-based computing solutions for digital document signing and completion. This approach helps in replacing labor-intensive paper
