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Features a company that works with biotechnology companies to identify potential animal health applications for their innovations and with animal health companies to identify new platform technologies and compounds for their pipelines.
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Veterinary clinical contract research, including pivotal and post-marketing studies Regulatory affairs (FDA CVM, USDA, EPA), including GMP manufacturing regulations Data management, including SAS
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Date Added: Mar 1, 2011 Hits: Rating: 0.00 Votes: 0
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Provides customized clinical software development, services, and system validation for the biopharmaceutical, emerging biomedical technology and healthcare industries.
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biotechnology, biopharmaceutical, medical devices, FDA, regulatory affairs, HIPPA, 21CFR11, clinical research organizations, CRO, clinical trial, data management systems
Coderant is a full-service Data Management company focused on the Life Sciences. in 1997, and headquartered in San Jose, California, Coderant provides access to a team of professionals dedicated to

Date Added: Mar 1, 2011 Hits: Rating: 0.00 Votes: 0
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Assists sponsors of investigational drugs and medical devices by centralizing all IRB submission activities and producing timely, diligent reviews of clinical research.
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Liberty Institutional Review Board (IRB) is an independent, central institutional review board located in Deland, Florida. With the ability to review all types of research, Liberty IRB produces timely, diligent reviews of clinical research.
Liberty IRB is a diverse independent institutional review board (IRB). Our passion is protecting the rights and welfare of human research subjects by ensuring the risks never outweigh the value of

Date Added: Mar 1, 2011 Hits: Rating: 0.00 Votes: 0
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assist manufacturers in bringing new medical technologies to the European market efficiently and cost-effectively
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MedPass International Medical Device CRO: Specialists in Clinical Development, Regulatory Strategies and EU Market Access for Medical Devices MedPass International is your Partner in the EU for medical devices Regulatory, Reimbursement and CRO Services
ADVANCING MEDICAL DEVICE TECHNOLOGIES MedPass is the largest, independent, full service CRO specialised in the European medical device market. We are a “one stop shop” for medical device

Date Added: Mar 1, 2011 Hits: Rating: 0.00 Votes: 0
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Contract research organization offering regulatory, pre-clinical, and clinical trial services for medical devices.
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FDAnews: Postmarket Is CDRH's Top Priority, Official Says Of all CRO's listed in the Applied Clinical Trials, Factory is the only CRO outside the US, specialized in Medical Devices Factory is not
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Date Added: Mar 1, 2011 Hits: Rating: 0.00 Votes: 0
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