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Clinical Trial Document Management Services

    
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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.
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...
 
Document Storage As with any clinical trial, large volumes of paper data are created. After the trial has been completed, regulatory and legal guidelines require these...
 
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...
BioClinica, Inc.  BioClinica delivers world class electronic data capture, medical imaging management and data management solutions that increase efficiency and decrease costs through all stages of the clinical development life cycle.
 
BioClinica WebSend BioClinica WebSend offers key benefits over the manual transport methods commonly used in imaging trials.
 
CDISC Implementation Modern clinical research requires that biopharmaceutical companies, medical device companies, and their partners easily be able to exchange and review...
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.
 
Electronic Source Record (ESR) 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 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.
 
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...
Symphony Clinical Research formerly known as Clinical Resource Network, LLC  Symphony Clinical Research formerly known as Clinical Resource Network, LLC (CRN) provides in-home clinical services. By taking trial visits to subjects in their homes, convenient participation yields enrollment,...
Reliance Clinical Research Services  RCRS, a CRO offers Preclinical Development, Phase I-IV Clinical Trial Management, Bioequivalence, Pharmacokinetic & Pharmacodynamic studies and Cardiac Safety studies, Pharmacovigilance, Biometrics, Regulatory Affairs,...
 
Phase 1 Clinical Trials Clinical Trials
 
Phase II-IV Clinical Trial Management and Monitoring Clinical Trial Management and Monitoring
Dolby Research  Dolby Research LLC is a full service Contract Research Organization (CRO) which offers a complete range of clinical development and consulting services to the pharmaceutical, biotechnology, and medical device industries....
 
Clinical Trial Research Services & Therapeutic Areas Our team is headed by a board certified urologist, board certified endocrinologist, and certified semen analyst, who vigorously apply their expertise to...
Premier Research Group  Premier Research is a leading global solutions-driven CRO committed to therapeutic focus and operational expertise to deliver clinical trial services of the highest quality for biopharmaceutical and medical device...
Fortitude Clinical  Fortitude Clinical. Clinical Research Organisation (CRO), Site Management Organisation (SMO), and Generic Product Services in Asia Pacific. Headquartered in Singapore.
Onorach Clinical  We focus on the unique challenges of drug, biopharmaceutical and medical device development and offer clients a full range of services to efficiently and cost-effectively manage the clinical trial development process.
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Clinical Trial Document Management Services Research Library

Allphase Clinical - Risky Business
Allphase Clinical Research
Executing a clinical development program without sufficient resources, experience, and planning is akin to starting a war armed with a pea-shooter. This is a trend that has been developing during these recession plagued years. Despite the counter-intuitiveness of the approach, one can sympathize given the incessant ticking of the patent clock and the difficulties in securing and maintaining ...
 
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 ...
 
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 ...
 
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.
 
Sanofi Expects Online Collaboration to Save Millions of Euros
NextDocs Corporation
Sanofi relied on time-consuming, paper-based processes to manage global drug trials. The logistics of managing this process for dozens of concurrent trials, with over 25,000 documents each, was daunting. To lower costs, reduce the risk of errors, and improve compliance, sanofi deployed a clinical trial portal based on SharePoint. The new solution will accelerate time-to-market for new drug ...
 

Clinical Trial Document Management Services Video

BioClinica Trial Blazers eClinical Technologies BioClinica, Inc. Experts from BioClinica explain some of the ways that eClinical is more than just technology.
 
Momentum Scheduling Demo Bio-Optronics Inc.
 
Clinical Trial Document Management Services BioClinica, Inc. Products

Clinical Trial Document Management Services News

Clinical Trial Document Management Services Translational Drug Development (TD2) Information
Clinical Trial Document Management Services Clinical Ink Information
Clinical Trial Document Management Services Bio-Optronics Inc. Products
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