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Clinical Trial Data Management

    
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Clinical DataFax Systems Inc.  You have options. Use our Clinical Data Management Software as a service (SaaS), or self-host it on your own server; use our convenient EDC web portal from a browser or download our internet EDC app for outstanding...
 
DF ATK FDA requirements for research studies submitted for regulatory review include the need to validate the software used to collect and manage patient data. The...
 
DF Send Capture CRFs and other patient documents as well as data.
 
Allphase Clinical Research  Allphase Clinical Research is a clinical stage full-service Contract Research Organization (CRO) specializing in Respiratory, Oncology, Cardiovascular and CNS. Over the last 12 years we have run over 150 trials for small...
 
Data Management Allphase Clinical Research offers a full spectrum of data management services and expertise to ensure the efficient and appropriate management of your...
 
Operational Support Our Clinical Operations Associates (COAs) fill a crucial supportive role to all members of the team. COAs work to streamline the process of managing a...
Bio-Optronics Inc.  Bio-Optronics is leading the way in healthcare workflow software. We provide a family of clinical trial management systems (CTMS), staff and physician scheduling solutions and products for patient ID, registration, and...
 
Clinical Conductor™ Enterprise CTMS Collaborative workflow software for SMOs, CROs, sponsors and sites.
 
Clinical Conductor™ Site CTMS Comprehensive workflow software for clinical trial sites.
Clinical Ink  Clinical Ink’s FDA compliant eSource technology replaces EDC and CRFs, eliminates SDV, and enables real-time data availability and remote monitoring of clinical trial data.
 
ChartRoom™ Access to source data is securely controlled via our ChartRoom™. Before a source document can be modified, it must be checked out and downloaded to a...
 
SureSource Clinical Ink offers an Electronic Source Record (ESR) for clinical trials that provides cleaner data more quickly — saving money by eliminating SDV,...
Translational Drug Development (TD2)  Translational Drug Development (TD2) is a biopharma service provider uniquely positioned to meet your development challenges. TD2 integrates world-class clinical and regulatory expertise with "-omic" science and provides...
 
Clinical Services TGen Drug Development (TD2) is uniquely positioned to ensure that your clinical trial development plan is a commercial success by providing the strategic...
 
Clinical Trial Management TD2's drug development team has successfully led the oncology drug programs of numerous pharmaceutical and biotechnology companies. Our project managers...
MedNet Solutions  MedNet Solutions provides web-based eClinical solutions - electronic data capture (EDC), clinical trial management (CTMS), and investigator initiated trial (IIT) managment systems - for pharmaceutical, medical device and...
 
EMPOWER - MedNet’s comprehensive investigator initiated trial (IIT) management solution that automates IIT submissions, management, and reporting.
 
ENLIGHTEN - MedNet’s proven, fully customizable eClinical solution that delivers the vital EDC, CTMS and CDMS functionality you need for success.
 
Medidata Solutions  Medidata's advanced cloud-based platform lowers the total cost of clinical development by optimizing clinical trials from concept to conclusion.
 
Medidata CTMS™ Medidata CTMS™ automates site management workflows and handles operational complexities with ease—from study start-up to site payments, and site monitoring...
PRC Clinical  PRC Clinical offers a full suite of world-class CRO services for Phase I -IV clinical trials. We are headquartered in the San Francisco Biotech corridor and serve virtual, small and mid-size pharma/biotech and medical...
Lifetree Clinical Research  Lifetree is a 60 bed Clinical Research Organization with expertise in Phase 1 (first in human) research, drug development, clinical trial management, and neuroscience research. Visit our site to view all of our services...
Novella Clinical  Novella Clinical is a full service clinical research organization dedicated to clients in the oncology, medical device and biopharmaceutical industries. For over a decade Novella has served as a trusted outsourcing...
 
Oncology Expertise Prologue Research provides a full range of clinical trial services – from protocol design to FDA submission – in order to speed your drug or device to...
Worldwide Clinical Trials, Inc.  Worldwide Clinical Trials is a global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract...
 
Services While Worldwide Clinical Trials supports you in your pre-registration through peri-approval studies, our sister division, Worldwide Clinical Trials Drug...
SGS Life Science Services - Clinical Research  SGS Life Science Services has over 35 years of experience as a global contract service organization providing integrated solutions from preclinical activities to Phase I-IV clinical trials, and bioanalysis.
 
Clinical Data Management Services At SGS, we have over 15 years’ experience in providing unparalleled clinical data management services. Our Data Managers play a key role in each clinical...
Theorem Clinical Research  Established in 1985, Theorem Clinical Research is one of the industry’s leading full-service, global CROs. Theorem provides core CRO services for Phases I to IV, but with niche business units in the areas of Technical...
 
Early Phase Clinical Trials Whether your project is standard or complex, our Early Phase Business Unit (Phase I/IIa) has a dedicated, streamlined approach that helps ensure we complete...
 
Phase II/III Clinical Trials As a mid-sized CRO, we consider ourselves to be the “right size” outsourcing partner. While we are small enough to provide you with a personal touch and...
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Clinical Trial Data Management Research Library

The High Cost of Choosing the Wrong CTMS
Bio-Optronics Inc.
June 2012 A CenterWatch Article Reprint Volume 19, Issue 06 By Michael Bonavilla T oday’s clinical research sites are no strangers to clinical trial manage- ment systems (CTMS) or other com- puterized processes used to oversee trials. One of the most important aspects of a clinical trial, and one that must be man- aged well, is its finances. While the first step in overseeing trial finances is ...
 
SGS Life Science Services Uses Medidata CTMS™ to Cut Site Payment Process Times by Over 60 Percent
Medidata Solutions
With sites under increasing economic pressure, timely payments are critical to keeping them focused on patient enrollment. However, many sponsors and CROs are challenged to address high volumes of invoices and complex payment requests with manual processes. SGS Life Science Services found a dramatically better way using Medidata CTMS.
 
PCRT Case Study: Setting a New Standard for Pancreas Cancer
Translational Drug Development (TD2)
PCRT Case Study: Setting a New Standard for Pancreas Cancer A Phase I-II study using gemcitabine + nab-paclitaxel in advanced Pancreatic Cancer Patients Pancreatic cancer is the fourth leading cause of cancer death and has devastatingly low 1 and 5 year survivorship rates. Here's how are team is making a difference: In 2006, the Pancreatic Cancer Research Team (PCRT), led by Dr. Manuel Hidalgo ...
 
Meeting the Real-Time Informational Needs of a Successful Clinical Trial
Bio-Optronics Inc.
This article describes the benefits achieved during one contract research organization’s (CRO’s) implementation of an enterprise CTMS, focusing on real-time exchange of information among the CRO, sponsors, and sites. l e a r n i n g o B j e c t i v e At the conclusion of this course, participants should be able to identify informational needs for their organization and plan for selection and ...
 
Medidata Clinical Cloud White Paper
Medidata Solutions
This white paper describes how the Medidata Clinical Cloud™ transforms clinical research by delivering instantaneous global access to advanced technology, data and analytics. It also shows how the platform can enable a potential $33M in savings and revenue acceleration for a typical Phase III trial.
 

Clinical Trial Data Management Video

Clinical Ink's SureSource® Demonstration Clinical Ink Clinical Ink's demo is highly informative and in 13:00 minutes can give you a better understanding of eSource Technology. SureSource eliminates SDV, ...
 
Clinical Conductor Site CTMS Testimonial Pensacola Research Bio-Optronics Inc. Bio-Optronics interviewed Clinical Conductor customer Michael Ellis, Site Director at Pensacola Research Consultants.
 
Clinical Trial Data Management Clinical Ink Pharmaceuticals

Clinical Trial Data Management News

Clinical Trial Data Management Clinical DataFax Systems Inc. Pharmaceuticals
Clinical Trial Data Management Translational Drug Development (TD2) Pharmaceuticals
Clinical Trial Data Management Bio-Optronics Inc. Information
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