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Phase II Clinical Trial

    
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Myriad RBM, Inc.  Myriad RBM is a CLIA-certified biomarker testing laboratory specializing in cost-effective, high-quality multiplexing services. Our protein immunoassays benefit drug discovery & development from preclinical through Phase...
 
Services Provided Myriad RBM, Inc. is the world’s leading multiplexed immunoassay testing laboratory, providing comprehensive protein biomarker services based on its...
BioScience Laboratories, Inc.  A FDA / EPA registered, GLP and GCP, Microbiology, Virology, Toxicology analytical testing facility providing product safety / efficacy / custom testing, product development, product differentiation, and regulatory...
 
Microbiology Testing Laboratory Scientists in our Microbiology Laboratories are well-trained on ASTM, AATCC, AOAC, CLSI, and EN standard methods.
 
Testing Services Comprehensive microbiology, virology, toxicology Testing Services
Metrics Contract Services  Metrics Contract Services is a CDMO offering contract pharmaceutical research, pharmaceutical development, clinical trial and commercial manufacturing services. Metrics provides FTIM development and Phase I, II and III...
 
Clinical Trial Manufacturing Easy as Phase I, II, III — Clinical Trial Manufacturing at Metrics. Metrics offers the experience and expertise to handle manufacturing for oral dosage...
 
Formulations Development Metrics provides pharmaceutical product development including pre-formulation studies, formulation development, Clinical trial batch manufacturing and...
Clinovo  Clinovo is a leading-edge provider of cloud-based eClinical software headquartered in the Silicon Valley. Clinovo streamlines clinical trials by offering a Free, Validated, Do-It-Yourself Electronic Data Capture system,...
 
Electronic Data Capture - ClinCapture ClinCapture is the Only Free Validated EDC on the market.
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...
 
iMedNet EDC - MedNet’s innovative, SaaS-based eClinical solution that allows you to quickly, easily, and affordably configure your own studies.
Orban Biotech, LLC  The Company was founded with the mission of developing and commercializing a novel therapeutic vaccine to treat and prevent Type 1 Diabetes Mellitus (T1DM). The Company's drug is result of the many years of research by...
 
Insulin B Chain Vaccine The Phase I trial has been successfully completed under an IND that was cleared by the FDA. The Phase I trial was funded by the NIH and sponsored and...
Clinical Trials Management Solutions  CTMS Inc. is a Site Management Organization (SMO) that work with a network of qualified and experienced PI s. We provide safe and cost effective management of clinical trials through strict adherence to ICH/GCP...
xCeleron  Founded in 1997 in York, UK, Xceleron provides bioanalytical Accelerator Mass Spectrometry (AMS) services for accelerated early drug development. The company uses ultra-sensitive AMS to investigate the pharmacokinetics...
 
Low Level Human ADME/Mass Balance Studies There are times when a traditional 14C study is not adequately supported by liquid scintillation counting. In these circumstances the analytical needs of...
AtCor Medical  AtCor Medical offers the global gold standard in technology and support services for noninvasive measurement of central blood pressure and pulse wave velocity in clinical trials: SphygmoCor systems, investigator site...
Marsala Biotech Inc  Marsala Biotech Inc.- Head and Neck Cancer Gene therapy
MKPSPE  We provide End-to-End Pharmacovigilance related services. We process ICSRs from Phase I to IV clinical trials. Our experts are thorough with US, European and Japanese regulations. Medical writing related activities in...
Endpoint Research  Endpoint Research is a full service Clinical Research Organization founded in 1990. We provide Phase I/II to IV clinical development services to pharmaceutical, biotechnology and medical device companies in most major...
Kendle International Inc  Kendle International Inc. (Nasdaq: KNDL) is a leading global clinical research organization providing the full range of early- to late-stage clinical development services for the world's biopharmaceutical industry. Our...
 
Early stage We are unrivaled in our ability to run successful studies at the early stages of a product’s lifecycle. We know how important it is for you to reach an...
 
Late stage n the competitive and fast-moving world of clinical development, you need a CRO partner that will focus on delivering efficiencies and consistent value....
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Phase II Clinical Trial Research Library

Toxicology
Myriad RBM, Inc.
Learn how Myriad RBM's biomarker services can help provide a sensitive and early method for the detection of kidney injury. Nephrotoxicity or acute kidney injury is a major problem in both the preclinical and clinical setting that results in the failure of candidate compounds throughout the drug-development cycle. The kidney is particularly susceptible to drug induced toxicity since components ...
 
CDISC for Medical Device Companies
Clinovo
The healthcare industry, as well as regulatory bodies, has been hard at work in the standardization of clinical trial data. The need for data transparency, traceability, and auditability has continued to increase, in line with the cost of studies and the amount of data submitted to the FDA. As a result, much progress has been made in the past decade in creating standards to ease data exchange and ...
 
Using SAS® to Determine Sample Sizes for Traditional 2-Stage and Adaptive 2-Stage Phase II Cancer Clinical Trial Designs
Scian Services, Inc.
In a Phase II clinical trial, the primary objective is to determine the efficaciousness of a drug, such that decisions to proceed with further studies and development of the drug are warranted. To detect a measurable effect in an investigation product, a two-stage design is often used, whereby an interim look at the data may result in the decision to terminate the trial early, or proceed with the ...
 
Benefits and Challenges of EDC adoption
Clinovo
Clinical research is one of the most expensive areas of drug development. Bringing an approved new drug from initial private investment to a patient takes over 13 years and $1.3 billion, or an average of $146 million per year.1 Industry data shows that clinical trials costs are growing across all development phases. A 2011 report, Clinical Operations: Benchmarking Per-Patient Costs, Staffing and ...
 
Highly Automated ECG Analysis
Celerion
The finalization of the International Conference on Harmonization (ICH) E14 “Guidance for Industry: Clinical Evaluation of QT/QTc Interval Prolongation and Proarrhythmic Potential for Non-Antiarrhythmic Drugs” in 2005 changed expectations for evaluating cardiac safety in pharmaceutical development1. This guidance was created after several compounds linked to the potentially fatal cardiac ...
 

Phase II Clinical Trial Video

Meet Metrics Contract Services Metrics Contract Services
 
iMedNet EDC - an eClinical Solution MedNet Solutions iMedNet EDC is an innovative, SaaS-based eClinical technology platform that allows non-technical sponsor and CRO personnel to quickly, easily and ...
 
Phase II Clinical Trial BioScience Laboratories, Inc. Information

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