| Clinical Drug Trial Consultants Pharmaceuticals_and_biotechnology > Clinical trials > Clinical Drug Trial Consultants |  |
A clinical outcomes research company, offering consultancy, training and publications.
Works with several pharmaceutical companies testing investigational medications using volunteer patients from our study physicians as well as referrals from other physicians in the area, patient recruitment posters, commercials, as well as inter.
Clinical research services include project facilitation and management, contract staffing, investigational site management, and process advising
The World Center for Clinical Research is dedicated to exploring the issues surrounding clinical research in the pharmaceutical and biotechnology industries worldwide.
Services in registrations, clinical trial management and contacts within regulatory agencies throughout the world.
Consultation on clinical research development and conduct.
Provides clinical trials management and support to pharmaceutical and biotechnology companies for phase II-III drugs and medical products under FDA review, and post marketing studies.
A central laboratory, providing drug development laboratory services, from preclinical method development through to phase IV. GLP certified
Full-service site Management Organization that conducts Phase I through Phase IV clinical trials in various therapeutic areas covering the full range of medical and scientific inquiry.
Lineberry Research Associates offers clients a full range of services including consulting for all aspects of drug development, a complete scope of clinical research services and a variety of scientific writing and communications capabilities.
Provides personnel and training to support clinical research.
National Genetics Institute is a licensed clinical laboratory specializing in infectious disease clinical trials (HIV, HCV, HBV, HAV, PARVO, CMV, SIV, HDV, HGV) for the worldwide pharmaceutical industry.
Clinical contract research organization, with services in data management, statistics, development and regulatory affairs.
Clinical research organization (CRO), providing clinical research for pharmaceutical industry and biotechnology industry.
Established in 1982, Chiltern has amassed extensive experience in running trials from Phase I to Phase IV and across a broad therapeutic range.
Combination of on-site quality research, physician and member education, and the integration of clinical knowledge and pharmacoeconomics.
Serving the pharmaceutical, medical device and consumer product industries in the areas of preclinical and early clinical evaluation, safety assessment, statistics and risk assessment.
Specializes in the design and implementation of IVRS randomization systems to support the growing number of clinical trials in the biotech and pharmaceutical industries.
Provider of clinical development, regulatory affairs, licensing and communications consulting services to the pharmaceutical and medical device industries.
Consulting firm focusing on statistical analysis, application development and clinical trial management.
Provider of Phase II-IV clinical trials services delivering investigator selection, patient recruitment and study management services for pharmaceutical, CRO, and biotechnology industries.
Full range of clinical trials consultative services.
To assist companies in clinical monitoring, data analysis, and niche services with an objective of accelerating product development.
Global organization formed scientists and clinical trial experts to work with biopharmaceutical and medical device companies on expediting drug development by applying imaging and biomarker technologies.
Offers services in the scientific evaluation of treatments, such as the planning of clinical trials, the conduct of clinical trials and the reporting of results.
A contract research organization specializing in clinical monitoring, project management, contract staffing, and pharmacoeconomic studies for pharmaceutical, biotechnology, and medical device companies.
| Nb of links = 26 |