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
