AREAS OF STUDY Sample Clauses

AREAS OF STUDY. The committee will review Affirmative Action issues, including: a. Personnel Practices: such as assignment, recruitment, hiring, promotion, leadership training, retraining incentives and programs, and in-service; b. Curriculum and Resources: such as specific teaching resources, guidelines for selection of material, and necessary in-service; and c. School and District Environment: such as the equality of opportunity for students, curricular and extra-curricular activities, policy on discrimination, and equality of access to all programs and services.
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AREAS OF STUDY. The committee will review Affirmative Action issues, including:
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AREAS OF STUDY. The licensing for the shared model for the four programs is t4,995 for one calendar year of unlimited access and users. January 1st - 2021 - December 31st, 2021.
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AREAS OF STUDY. The main goal of this residency program is to provide the resi- dent an organized and comprehensive experience to enable him/her to acquire the knowledge and skills in the evaluation and management of patients with neurosurgical complaints. The resident will also gain an appreciation for the collabora- tive efforts between other specialties. NEUROINTERVENTIONAL: The goal of the neurointerventional surgery rotation is to pre- pare and learn the role of minimally invasive procedures guid- ed under fluoroscopic control has radically changed the prac- xxxx of vascular neurosurgery in the last two decades. Multiple clinical studies and the continuous creativity of leaders in endovascular techniques have allowed the establishment of well defined therapeutic strategies using interventional neuro- radiology techniques for the management of cerebrovascular disease. PEDIATRIC NEUROSURGERY: The goal of the pediatric neurosurgery rotation is to prepare the neurosurgery residents to care for patients with pediatric head injuries. SKULL BASE NEUROSURGERY: The goal of the neurotology lateral skull base surgery rotation is to provide advanced education in the diagnosis and man- agement of disorders of the temporal bone, lateral skull base, and related anatomical structures, as well as advanced diag- nostic expertise and advanced medical and surgical manage- ment skills in neurotology. Surgery of the lateral skull base involving the mesial aspect of the dura or intradural structure requires the joint effort of a neurotology and neurological sur- xxxx team. Residents are trained in surgery and postoperative care of patients undergoing lateral skull base surgery and work in close collaboration with the neuro-logical surgery team. During education, residents gain exposure to new re- search opportunities and have time to explore new research ideas. SPINAL DISORDER: The primary goal of the spinal disorders rotation is prepara- tion of the neurosurgical resident to treat adult spinal cord injuries. CEREBROVASCULAR/ENDOVASCULAR The goal of the cerebrovascular/endovascular rotation is to pre-pare neurosurgical residents to care intracranial aneu- rysms, and subarachnoid hemorrhages. STEREOTACTIC/IMAGE-GUIDED/FUNCTIONAL The goal of this rotation is to obtain a history and physical examination on a patient with Xxxxxxxxx'x disease, essential tremor, or epilepsy. RESIDENT ELIGIBILITY: Applicants with one of the following qualifications are eligible for appointment to accredited resid...
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Related to AREAS OF STUDY

  • Development Plan document specifying the work program, schedule, and relevant investments required for the Development and the Production of a Discovery or set of Discoveries of Oil and Gas in the Concession Area, including its abandonment.

  • Work Plan Coordinate a work plan including a list of the proposed meetings and coordination activities, and related tasks to be performed, a schedule and an estimate. The work plan must satisfy the requirements of the project and must be approved by the State prior to commencing work.

  • Development Work The Support Standards do not include development work either (i) on software not licensed from CentralSquare or (ii) development work for enhancements or features that are outside the documented functionality of the Solutions, except such work as may be specifically purchased and outlined in Exhibit 1. CentralSquare retains all Intellectual Property Rights in development work performed and Customer may request consulting and development work from CentralSquare as a separate billable service.

  • Research Plan The Parties recognize that the Research Plan describes the collaborative research and development activities they will undertake and that interim research goals set forth in the Research Plan are good faith guidelines. Should events occur that require modification of these goals, then by mutual agreement the Parties can modify them through an amendment, according to Paragraph 13.6.

  • Development Phase contractual phase initiated with the approval of ANP for the Development Plan and which is extended during the Production Phase while investments in xxxxx, equipment, and facilities for the Production of Oil and Gas according to the Best Practices of the Oil Industry are required.

  • Development Program RWJPRI shall be [**] and have [**] in consultation with the JDAC, to select LICENSED COMPOUNDS which shall then be designated PRODUCTS for further DEVELOPMENT by RWJPRI and marketing by ORTHO and its AFFILIATES. RWJPRI shall provide KOSAN with written notice of its decision to select a LICENSED COMPOUND for DEVELOPMENT. Once a PRODUCT has been selected for further DEVELOPMENT, RWJPRI, with the advice of the JDAC, shall have the [**] right to develop the PRODUCT through STAGES O, I, II and III and shall have the [**] right to prepare and file, and shall be the owner of, all applications for MARKETING AUTHORIZATION throughout the world. During such DEVELOPMENT efforts, KOSAN will assist RWJPRI as may be mutually agreed, at RWJPRI's expense, in chemical development, formulation development, production of labeled material and production of sufficient quantities of material for STAGE O and initial STAGE I studies. RWJPRI shall exercise diligent efforts, commensurate with the efforts it would normally exercise for products with similar potential sales volume and consistent with its overall business strategy, in developing such PRODUCT in accordance with the DEVELOPMENT PLAN established by RWJPRI. In the course of such efforts RWJPRI shall, either directly or through an AFFILIATE or SUBLICENSEE to which the license shall have been extended, take appropriate steps including the following: (i) in consultation with the JDAC, select certain LICENSED COMPOUNDS for STAGE O DEVELOPMENT; and (ii) establish and maintain a program reasonably designed, funded and resourced to obtain information adequate to enable the preparation and filing with an appropriate and properly empowered national regulatory authority all necessary documentation, data and [**] CERTAIN INFORMATION IN THIS EXHIBIT HAS BEEN OMITTED AND FILED SEPARATELY WITH THE COMMISSION. CONFIDENTIAL TREATMENT HAS BEEN REQUESTED WITH RESPECT TO THE OMITTED PORTIONS. other evidence required for IND non-rejection to commence and conduct human clinical trials of such PRODUCT. (iii) proceed following IND non-rejection to commence PHASE I, II, and III clinical trials, associated studies and such other work which RWJPRI reasonably deems to be required for subsequent inclusion in filings for MARKETING AUTHORIZATION; (iv) after such submissions are filed prosecute such submissions and file all reasonably necessary, reports and respond to all reasonable requests from the pertinent regulatory, authorities for information, data, samples, tests and the like.

  • Study Population ‌ Infants who underwent creation of an enterostomy receiving postoperative care and awaiting enterostomy closure: to be assessed for eligibility: n = 201 to be assigned to the study: n = 106 to be analysed: n = 106 Duration of intervention per patient of the intervention group: 6 weeks between enterostomy creation and enterostomy closure Follow-up per patient: 3 months, 6 months and 12 months post enterostomy closure, following enterostomy closure (12-month follow-up only applicable for patients that are recruited early enough to complete this follow-up within the 48 month of overall study duration).

  • Research Project The findings of any research project, which would change the provisions of this Agreement will not be implemented until such changes are negotiated and agreed to by the parties.

  • Development Records Each Party shall maintain complete, current and accurate records of all Development activities conducted by it hereunder, and all data and other information resulting from such activities. Such records shall fully and properly reflect all work done and results achieved in the performance of the Development activities in good scientific manner appropriate for regulatory and patent purposes. Each Party shall document all non-clinical studies and Clinical Trials in formal written study reports according to Applicable Laws and national and international guidelines (e.g., ICH, cGCP, cGLP, and cGMP).

  • Study An application for leave of absence for professional study must be supported by a written statement indicating what study or research is to be undertaken, or, if applicable, what subjects are to be studied and at what institutions.

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