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Clinical Trial Document Management Services

    
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Bio-Optronics Inc.  Bio-Optronics is leading the way in healthcare technology. We provide clinical trial management systems (CTMS), staff and physician scheduling applications and products for patient ID, registration, and medications...
 
Clinical Conductor™ Enterprise CTMS The only enterprise CTMS capable of meeting any challenge related to managing multiple trials in multiple locations.
 
Clinical Conductor™ Site CTMS The CTMS Giving Sites All the Tools Needed to Raise the Bar in Clinical Research
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...
ePharmaSolutions  Rater Training, Clinical Trial Portal, Protocol Training, Site Feasibility, eTMF
 
Clinical Trial Portal (CTP) Investigator portals & study workspaces
 
RaterTrainer Innovative & affordable rater training, certification, & calibration solutions
 
Fisher BioServices  The leader in critical biological material management with expertise in biobanking & biorepository, cell therapy solutions, clinical trial sample management, Bio-API management, and cold-chain logistics.
 
Services Fisher BioServices offers global on-site or off-site biobanking service, clinical trial support, cell therapy solutions, biologic-API management, and cold...
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  Onorach Clinical manage Phase I to Phase IV clinical research studies for drug products, biologicals and medical devices. Onorach have a global reach and can work with clients of any size.
RUSSLAN Clinical Research, CRO  RUSSLAN Clinical Research is an independent European clinical trial management organisation offering a range of clinical research services to worldwide clients in the pharmaceutical, biotechnology and medical device...
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,...
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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 ...
 
Case Study – Patient Recruitment with Clinical Conductor Site CTMS at Accel Clinical Services
Bio-Optronics Inc.
Accel Clinical Services began using Clinical Conductor Site CTMS in the Fall of 2011. Prior to the implementation of Clinical Conductor Site CTMS, administrators and managers at Accel Clinical Services were using another CTMS system that did not have the functionality, usability or customer support that was required. This case study analyzes the organization, its challenges associated with these ...
 
Technology-driven clinical trial solutions: Low Back Pain
ePharmaSolutions
> 120 sites > 1000 patients > Low Back Pain Study Technology-driven clinical trial solutions ePharmaSolutions developed and deployed a highly effective patient recruitment campaign that yielded an outstanding number of qualified referrals, who were currently on a medication regimen, to support a low back pain study. ePharmaSolutions was selected to conduct patient recruitment services ...
 
Controlled-Rate Freezing of Cells During Ultra Cold Transit
Fisher BioServices
Patient cells that are isolated for development into a therapeutic product must be processed quickly or they lose their integrity and therapeutic value. Cells that cannot be processed immediately must be cryopreserved at -195°C in liquid nitrogen. However, to ensure viability and integrity upon thawing, freezing down to -195°C must be performed at a specific cooling rate, which requires ...
 
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 Document Management Services Video

User Management Application - Vendor Integration Manager ePharmaSolutions The UMA is a clinical trial user provisioning tool that simplifies the user account activation process for every major system used in clinical trials. ...
 
Clinical Conductor Enterprise CTMS Bio-Optronics Inc. Clinical Conductor Enterprise CTMS is a web-based, full-service CTMS that enables pro-active, portfolio-wide clinical trial management across all studies, ...
 
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