Our goal at Kentucky Clinical Research, Inc. (KCR) is to make the data management aspects of the clinical trials process efficient, affordable, and accessible to your company. We keep your goals in mind as we tailor our processes to fit your work environment. We are a small organization and as such we carefully evaluate each project to make sure that we are able to meet all the time requirements and, if need be, we refuse projects based on our existing commitments. We believe our clinical trials experience, streamlined data processes, and one-on-one attention offers our clients an affordable solution to the larger, more expensive Contract Research Organizations.
The Gelb Center utilizes the latest in maxillofacial imaging, Our Cone Beam CT (CBCT) allows 3 dimensional (3D) visualization of the temporomandibular joint and skull. The New Tom VG CBCT gives crystal clear images of the TMJs in sagittal, coronal and axial views. ENT/Sleep Studies One of the fastest-growing areas for CBCT scanning technology is among ENT physicians and surgeons. CBCT has, in an important sense, become the standard of care for this branch of medicine. Because they provide accuracy far superior to conventional cephalograms, CBCT scans are now used not only for diagnostic imaging for such conditions as ZMC fractures and other cranio-facial trauma, they're also used in intra-operative applications. One of the growing areas of application for this technology is CBCT-based surgical navigation. Now maxillo-facial surgeons can process the same 3D images they've utilized for diagnosis through software programs that can be used to guide them during surgery. CBCT imaging also enables dentists and ENT physicians to uncover other problems, such as air passage abnormalities, that are instrumental in causing such conditions as sleep apnea. As with many dental specialties, CBCT cephalometric imaging is changing the paradigm for ENT physicians and maxillo-facial surgeons. NewTom NNT analysis software enables the Gelb Center to realize the greatest benefit from three-dimensional CBCT images. It allows the dentist to perform initial diagnoses and subsequently to superimpose images for assessing growth, treatment changes, and the stability of treatment. The software supports the identification of such things as root inclination, positioning of impacted and supernumerary teeth, resorption, hyperplastic growth, and tooth structure anomalies. NewTom Implant Planning Software (NIP) enables The Gelb Center to utilize CBCT images to create detailed plans for performing implant surgery on your own personal computer. It provides accurate assessment of the thickness and morphology of bone at implant anchorage sites, as well as supporting unequaled quality panoramic, axial, and cross-sectional images. You can simulate the implant position on 3D models, identify the mandibular canal, draw panoramics and cross sections of the bone model, show the 3D bone model and calculate the bone density. Using NewTom Implant Planning the Dentist can plan the prothesis implant operation in a safer, more efficent and faster way.
Arkios BioDevelopment Int'l is a full service global biopharmaceutical consulting group, providing contract research services (CRO) to emerging technology companies developing new drugs, biologics, medical devices, and diagnostics. Our scope is two-fold:* To assist the emerging biopharmaceutical/device company with early stage regulatory strategic planning and implementation, culminating in the filing of a successful IND/IDE with the FDA. * To design and manage the clinical development of emerging technologies in the biopharmaceutical and device area, through successful product out-licensing or registration. Whether you are outsourcing a specific clinical trial management function, comprehensive regulatory affairs assistance, data management & biostatistics, need a Phase I center, or are seeking early stage product development guidance in approaching the FDA, Arkios can serve you. Founded in 1993 by Dr. Gary Pekoe, Arkios provides product development services for emerging technology companies in the biopharmaceutical industry. Clients in the emerging technology arena require focused, hands-on, reliable service the first time. We provide that to each and every client. The background of our people includes strong start-up biotechnology company experience, which means we understand the culture and environment of an emerging company. We understand terms like "burn rate," and know the importance of hitting corporate as well as developmental milestones. Arkios is divided into two functional areas: Early Stage Product Development Services and Phase II-IV Clinical Trial Management. Our Early Stage group conceives Strategic Regulatory Plans, develops and manages preclinical / pre-IND programs, writes and files INDs, and manages Phase I trials for our clients. In the Phase II-IV group, we provide full CRO services such as Clinical Trial Design & Management, Monitoring / Quality Assurance, full Regulatory Affairs consulting, Data Management, Biostatistics, Medical Writing, Investigator Location, and other tasks related to clinical product development. Items from this list are also available in a piecemeal consulting fashion.
CRM offers exceptional support to government and commercial organizations engaged in biomedical research. With a staff comprised of high-caliber professionals experienced in clinical trial design and management, clinical database management systems, statistical support, and regulatory compliance, CRM can help expedite your product development process towards licensure. We believe our customers deserve the highest quality and commitment possible. Our services will be provided within the time frame required and at a reasonable and fair cost. We recognize that each customer's needs are unique, and we strive to provide innovative, responsible and effective solutions. CRM can support programs with service requirements in the following areas:
Reliance Clinical Research Services (RCRS) is a full-service Contract Research Organization based in Mumbai, India. RCRS provides a broad range of clinical research services to assist pharmaceutical companies in bringing new products to the market. RCRS offers the domestic and international pharmaceutical, biotechnology and medical device companies, services at extremely competitive and affordable costs. We utilize the infrastructure of our parent company Reliance Industries Limited for the coordination of clinical trials activities; the benefits of the costs savings are passed on to our clients. RCRS has the advantage of offering the entire gamut of pre-clinical, clinical and post marketing services within the same comprehensive project management systems, thereby ensuring a smooth flow of data between paper and electronic reportoires with a high adherence to quality control. Each of our services are governed by rigorous Standard Operating Procedures and Policies which adhere to the more stringent of ICH-GCP and applicable regulatory guidelines. RCRS is proud of its role in helping sponsors achieve success in improving healthcare. We believe the following attributes define future Leadership in RCRS: Customer centricity Initiative and an attitude of ownership Passion for excellence and ability to motivate team Problem solving and an innovative "can do" mindset Entrepreneurship and stretch Today RCRS offers challenging assignments and career opportunities to candidates with expertise in the field of clinical research in the areas of Clinical Operations, Regulatory, Information Technology, Biometrics, Medical Affairs, Quality Assurance and Pharmacovigilance. RCRS offers its employees a challenging career and performance based financial and other growth incentives and perks. The Human Resources department utilizes modern tools and innovative methods to assess the performance of each of its staff members thus making the growth process transparent. Employees of RCRS are part of a happy and satisfying environment. RCRS offers its employees cross functional roles which enhances their intellectual growth. Please provide your resume so that as and when we find suitable opportunities we could contact you based on our review of your profile. We invite you to join us in creating an exciting future and to build a career in clinical research with the unique mission of "Bringing Research To Life".
Advanced Clinical Research Services provides the expertise and responsiveness you expect from a data management partner. We customize our support around your specific project and requirements. We supplement our full-time experienced professionals with temporary staffing so that we can expand or contract to meet your changing needs. Plus, we provide ongoing in-house training on new software and new aspects of studies to assure our professionals meet or exceed client needs. Our goal is to be an extension of your data management team.
http://www.symbionresearch.com
Symbion Research International, Inc., was founded in 1995, with the principal purpose of providing superior client-individualized contract research services to biotechnology, pharmaceutical, and device companies. Symbion is a full-service contract research organization (CRO), offering a complete spectrum of strategic and product development, clinical research, and regulatory services to U.S. and international clients. We are a value-driven company committed to making a real difference. Our mission at Symbion is to provide exceptional value to our clients by enabling them to accelerate their product development cycle. We accomplish this by providing high-quality, cost-effective, customized, innovative, and timely strategic planning, preclinical, regulatory, and clinical research services. The Symbion philosophy always is to become a true partner in development, assimilating the client's goals and making the distinction between Symbion and each client as transparent as possible.
http://www.endpointresearch.com
Endpoint Research is a full service Clinical Research Organization founded in 1990. We provide Phase I to IV clinical development services to pharmaceutical, biotechnology and medical device companies in most major therapeutic areas, with a strength in complex indications, particularly oncology and respiratory. Endpoint has been an international CRO since 1998 when we opened our office in the United Kingdom. We have continued to expand our geographic reach and service offerings by opening our US office and implementing full, Oracle Clinical-based clinical data management, Medical and Consulting services. Our head office is in Toronto, Canada with operational offices in Houston, Texas and Bells Hill, Scotland. Endpoint provides full clinical trial services (study design, management, monitoring, data handling and statistical services) for clinical trials in North America and Europe, including Eastern Europe. Endpoint Research provides clinical research services from Phase I to regulatory submission. We have very strong capabilities in two therapeutic areas in particular:
Perceptive is a subsidiary of PAREXEL International Corporation, one of the world's largest biopharmaceutical outsourcing organizations. PAREXEL's commitment to comprehensive services resulted in the creation of an advanced technology group. That group, now Perceptive, developed new technologies, acquired some best of breed business applications and is busy anticipating next generation solutions. Perceptive now seeks new ways of applying technology to the drug development process, including developing and / or licensing technology tools. Perceptive's knowledge of the industry is fuelled by its relationship with PAREXEL (to whom it continues to supply software and services). Perceptive's understanding of technology's expanding role sets it apart. As a result, Perceptive sets the standard for the use of technology in clinical trials.
Clinical Data, Inc. operates its business in two segments: PGxHealth and Cogenics. As PGxHealth, the Company focuses on the development and commercialization of targeted therapeutics and predictive tests from its portfolio of biomarkers. As Cogenics, it provides genomic solutions to both the healthcare and life sciences industries. These solutions, including sequencing, gene expression, genotyping, biomanufacturing support, extraction, biobanking, and sample management are offered on a variety of platforms and are conducted in both regulated and unregulated environments. On August 23, 2007, the Company acquired Epidauros Biotechnologie A.G. On June 18, 2007, the Company sold Clinical Data Sales and Service, Inc. to Vital Diagnostics Holding Corp. On October 25, 2007, it sold Vital Scientific B.V. to the ELITech Group. On November 14, 2007, it sold Electa Lab s.r.l. to Vital Diagnostics B.V. In August 2008, the Company announced the acquisition of Adenosine Therapeutics, L.L.C.
Kendle International Inc. is a global clinical research organization (CRO) that provides a range of Phase I-IV global clinical development services to the biopharmaceutical industry. The Company augments the research and development activities of biopharmaceutical companies by offering clinical research services and information technology designed to reduce drug development time and expense. It delivers integrated clinical development services, including clinical trial management, clinical data management, statistical analysis, medical writing, regulatory consulting and organizational meeting management and publications services on a contract basis. Its Early Stage business focuses on the Company’s Phase I operations, while Late Stage is comprised of clinical development services related to Phases II through IV clinical trials, regulatory affairs and biometrics offerings. In June 2008, the Company announced the acquisition of DecisionLine Clinical Research Corporation.
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