Cenetron provides concierge project management and clinical trial site support to oversee every aspect of each clinical trial from beginning to end.
Offering clinical trial monitoring services from feasibility assessments, to site selection, site initiation and site qualification until site closeout visits.
MedTrials has a strong reputation as Clinical Trial Management experts. Our teams are qualified by training and experience with the required knowledge, skills, and abilities to successfully deliver reliable data from protected subjects on time and within budget. ...
Start your trial sooner with rapid patient recruitment and enrollment at our Columbus, Ohio-based independent clinical site. Streamline clinical trial management here.
A clinical trial management system (CTMS) is responsible for managing all operational aspects of a clinical trial, from study startup to closeout. Research sites, site networks, health systems, academic medical centers, and cancer centers use a CTMS to centralize information related to protocols, ...
Manage your Clinical Supplies and your entire Clinical Trial efficiently and seamlessly using our integrated and modularized solutions.
Learn more > Enable your staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant eSource + EDC system integrated with your clinical trial management system Learn more > Subscribe...
Manage your clinical trials with confidence, precision, and efficiency. Our cloud-based, customizable Clinical Trial Management System (CTMS) is designed for hospitals, transforming how to plan, budget, and execute trials. From start to finish, it meets the diverse needs of every role in clinical...
Enable your staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant eSource + EDC system integrated with your clinical trial management system Learn more >...
For treatment-resistant patients, a prospective treatment duration is required and should be potential (USA, eastern Europe, and Asia generally have the highest potential), prevalence ofthe From a management perspective, it is imperative to agree on timelines upfront and thePharmaceutical Industry...