High-technology Diagnostic Tests Sample Clauses

High-technology Diagnostic Tests. Immunohistochemistry. - Ergometrics, xxxxxx monitor, electrophysiological and therapeutic studies. - Amniocentesis and karyotypes. - Polysomnography. - Magnetic resonance imaging (MRI) and Computer- ised Tomography (CT scan). - Obstetricia y Ginecología: revisión ginecológica en cada anualidad de seguro, para la prevención del cáncer de mama, endometrio y cérvix. - Cardiología: incluye la prevención del riesgo coro- nario en personas mayores de 40 años. - Urología: revisión urológica en cada anualidad de seguro para la prevención del cáncer de próstata. - Planificación familiar: Control del tratamiento con anovulatorios, implantación de DIU y su vigilan- cia, incluyendo el coste del dispositivo. Ligadura de trompas y vasectomía. Queda expresamente excluida la interrupción voluntaria del embara- zo y las reducciones embrionarias, así como los tratamientos de esterilidad o infertilidad.
AutoNDA by SimpleDocs
High-technology Diagnostic Tests. Immunohistochemistry. - Ergometrics, xxxxxx monitor, electrophysiological and therapeutic studies. - Magnetic resonance imaging (MRI) and Computer- ised Tomography (CT scan). - CT colonography (exclusively in addition to fibro- colonoscopy owing to intolerance or stenosis and in patients with medical problems which rule out con- ventional fibrocolonoscopy). - CT coronarography (exclusively for patients with symptomatic heart disease with inconclusive stress test, in valve replacement surgery and in evaluating stenosis after coronary bypass surgery and in coro- nary tree malformations, not including under any cir- cumstances stenosis evaluation after stent implant, the use in quantification of coronary artery calcium and the use as a diagnostic screening test). - Nuclear medicine. PET/CT (Including exclusively those using the radiopharmaceutical 18F-FDG and in the clinical indications established in the fact sheet and with the authorization of the Spanish Agency for Drugs and Health Care Products).
High-technology Diagnostic Tests. Immunohistochemistry. - Ergometrics, xxxxxx monitor, electrophysiological and therapeutic studies. - Amniocentesis and karyotypes. - Polysomnography. - Magnetic resonance imaging (MRI) and Computer- ised Tomography (CT scan). - CT colonography (exclusively in addition to fibro- colonoscopy owing to intolerance or stenosis and in patients with medical problems which rule out con- ventional fibrocolonoscopy). - Cardiología: incluye la prevención del riesgo coro- nario en personas mayores de 40 años. - Urología: revisión urológica en cada anualidad de seguro para la prevención del cáncer de próstata. - Planificación familiar: Control del tratamiento con anovulatorios, implantación de DIU y su vigilan- cia, incluyendo el coste del dispositivo. Ligadura de trompas y vasectomía. Queda expresamente excluida la interrupción voluntaria del embara- zo y las reducciones embrionarias, así como los tratamientos de esterilidad o infertilidad.

Related to High-technology Diagnostic Tests

  • Human Leukocyte Antigen Testing This plan covers human leukocyte antigen testing for A, B, and DR antigens once per member per lifetime to establish a member’s bone marrow transplantation donor suitability in accordance with R.I. General Law §27-20-36. The testing must be performed in a facility that is: • accredited by the American Association of Blood Banks or its successors; and • licensed under the Clinical Laboratory Improvement Act as it may be amended from time to time. At the time of testing, the person being tested must complete and sign an informed consent form that also authorizes the results of the test to be used for participation in the National Marrow Donor program.

  • Diagnostic procedures to aid the Provider in determining required dental treatment.

  • Commercialization Intrexon shall have the right to develop and Commercialize the Reverted Products itself or with one or more Third Parties, and shall have the right, without obligation to Fibrocell, to take any such actions in connection with such activities as Intrexon (or its designee), at its discretion, deems appropriate.

  • Technology Discoveries, innovations, Know-How and inventions, whether patentable or not, including computer software, recognized under U.S. law as intellectual creations to which rights of ownership accrue, including, but not limited to, patents, trade secrets, maskworks and copyrights developed under this Agreement.

  • Technology Research Analyst Job# 1810 General Characteristics Maintains a strong understanding of the enterprise’s IT systems and architectures. Assists in the analysis of the requirements for the enterprise and applying emerging technologies to support long-term business objectives. Responsible for researching, collecting, and disseminating information on emerging technologies and key learnings throughout the enterprise. Researches and recommends changes to foundation architecture. Supports research projects to identify and evaluate emerging technologies. Interfaces with users and staff to evaluate possible implementation of the new technology in the enterprise, consistent with the goal of improving existing systems and technologies and in meeting the needs of the business. Analyzes and researches process of deployment and assists in this process.

  • Third Party Technology The Company makes use of third party technology to collect information required for traffic measurement, research, and analytics. Use of third party technology entails data collection. We therefore would like to inform clients the Company enables third parties to place or read cookies located on the browsers of users entering the Company’s domain. Said third parties may also use web beacons to collect information through advertising located on the Company’s web site. Please note that you may change your browser settings to refuse or disable Local Shared Objects and similar technologies; however, by doing so you may be disabling some of the functionality of Company’s services.

  • New Technology When new or updated technology is introduced into a workplace, it will be the responsibility of the employer to provide appropriate and, if necessary, ongoing training to the employees directly affected. Such training will include any health and safety implications or information that will enable employees to operate the equipment without discomfort and will help maintain their general well-being.

  • Research Use The Requester agrees that if access is approved, (1) the PI named in the DAR and (2) those named in the “Senior/Key Person Profile” section of the DAR, including the Information Technology Director and any trainee, employee, or contractor1 working on the proposed research project under the direct oversight of these individuals, shall become Approved Users of the requested dataset(s). Research use will occur solely in connection with the approved research project described in the DAR, which includes a 1-2 paragraph description of the proposed research (i.e., a Research Use Statement). Investigators interested in using Cloud Computing for data storage and analysis must request permission to use Cloud Computing in the DAR and identify the Cloud Service Provider (CSP) or providers and/or Private Cloud System (PCS) that they propose to use. They must also submit a Cloud Computing Use Statement as part of the DAR that describes the type of service and how it will be used to carry out the proposed research as described in the Research Use Statement. If the Approved Users plan to collaborate with investigators outside the Requester, the investigators at each external site must submit an independent DAR using the same project title and Research Use Statement, and if using the cloud, Cloud Computing Use Statement. New uses of these data outside those described in the DAR will require submission of a new DAR; modifications to the research project will require submission of an amendment to this application (e.g., adding or deleting Requester Collaborators from the Requester, adding datasets to an approved project). Access to the requested dataset(s) is granted for a period of one (1) year, with the option to renew access or close-out a project at the end of that year. Submitting Investigator(s), or their collaborators, who provided the data or samples used to generate controlled-access datasets subject to the NIH GDS Policy and who have Institutional Review Board (IRB) approval and who meet any other study specific terms of access, are exempt from the limitation on the scope of the research use as defined in the DAR.

  • Diagnostic Services Procedures ordered by a recognized Provider because of specific symptoms to diagnose a specific condition or disease. Some examples include, but are not limited to:

  • Research, Science and Technology Cooperation 1. The aims of cooperation in research, science and technology, carried out in the mutual interest of the Parties and in compliance with their policies, will be: (a) to build on existing agreements already in place for cooperation on research, science and technology; (b) to encourage, where appropriate, government agencies, research institutions, universities, private companies and other research organizations in the Parties to conclude direct arrangements in support of cooperative activities, programs or projects within the framework of this Agreement, specially related to trade and commerce; and (c) to focus cooperative activities towards sectors where mutual and complementary interests exist, with special emphasis on information and communication technologies and software development to facilitate trade between the Parties. 2. The Parties will encourage and facilitate, as appropriate, the following activities including, but not limited to:

Draft better contracts in just 5 minutes Get the weekly Law Insider newsletter packed with expert videos, webinars, ebooks, and more!