Clinical Practicum Sample Clauses

Clinical Practicum. During the clinical rotation training experiences, students perform hands-on advanced clinical training tasks under the supervision of an on-site clinical preceptor. The MLS Program and the student work together in identifying an appropriate clinical laboratory that will serve as a clinical training site. In some cases, more than one clinical training site may be needed to ensure all required competencies are taught and assessed. Training usually occurs on the first shift. Students may need to revise their work schedule or take time-off to complete clinical hours. Admission Period: Ivy Tech Community College students must be admitted to the UC College of Allied Health Sciences during the duration of this agreement (i.e. between May 2022 and May 2025). Agreement Execution Date: May 2022 Agreement End Date: May 2025 TRANSFER ARTICULATION AGREEMENT Ivy Tech Community College, Associate of Applied Science, Medical Laboratory Technology to University of Cincinnati, College of Allied Health Sciences, Bachelor of Science in Medical Laboratory Science (ONLINE)
Sample 1See All (5)
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Clinical Practicum. School shall be responsible for the development, implementation, and operation of the clinical component of its educational programs offered and conducted at CoxHealth pursuant to this Agreement (collectively referred to herein as the “Practicum”). Such responsibilities of School include the following:
Sample 1Sample 2
Clinical Practicum. During the clinical rotation training experiences, students perform hands-on advanced clinical training tasks under the supervision of an on-site clinical preceptor. The MLS Program and the student work together in identifying an appropriate clinical laboratory that will serve as a clinical training site. In some cases, more than one clinical training site may be needed to ensure all required competencies are taught and assessed. Training usually occurs on the first shift. Students may need to revise their work schedule or take time-off to complete clinical hours. DocuSign Envelope ID: E491D2D0-16A2-4BDC-B997-BA5E3F994A1E TRANSFER ARTICULATION AGREEMENT Xxxxx State College, Associate of Applied Science, Medical Laboratory Technology to University of Cincinnati, College of Allied Health Sciences, Bachelor of Science in Medical Laboratory Science (ONLINE) Admission Period: Xxxxx State College students must be admitted to the UC College of Allied Health Sciences during the duration of this agreement (i.e. between May 2022 and May 2025). Agreement Execution Date: May 2022 Agreement End Date: May 2025 EXECUTION, DURATION AND REVIEW OF AGREEMENT: This agreement becomes effective upon its signing by the Deans of both Colleges and will remain effective for three years. At the end of this time, the agreement will be reviewed and may be renegotiated. Xxxxx State College and the UC College of Allied Health Sciences agree to keep one another informed as program changes affecting the agreement occur. The Deans of both Colleges will agree upon any future additions and/or amendments to this document in writing. 8/3/2022 This agreement will be reviewed on an annual basis and is subject to change due to revisions in program curriculum. Xxxxx State College students are encouraged to work closely with their academic advisor to monitor possible changes. See attached appendix for course equivalencies and transfer degree map. Xx. Xxxx Xxxxxx-Xxxxxx, PhD Xxxxxxx and Chief Academic Officer Xxxxx State College Xxxxxxx Xxxxxxx, PhD, MLS(ASCP)cm Interim Xxxx College of Allied Health Sciences University of Cincinnati Xxxxxxx Xxxxxxx, MSTE, MT (ASCP) Program Coordinator, Medical Laboratory Technology Xxxxx State College Primary Contact Person for this Agreement: Xxxx Xxxxxx, MS, MLS (ASCP)cm Program Director, Medical Laboratory Science College of Allied Health Sciences University of Cincinnati Xxxxx State College University of Cincinnati Name Title Xx. Xxxx Xxxxxx-Xxxxxx, PhD Xxxxxxx ...
Sample 1
Clinical Practicum. The required clinical practicum is referred to as competency-based education. The curriculum is structured based on defined objectives and competencies. Clinical education is a planned and structured experience. The entire 20-month program is an inter-sequential integration of didactic and practical learning through classroom lectures, clinical laboratories, supplementary lectures, discussions, demonstrations, and supervised practice of standardized procedures. Clinical sites may be added or deleted at the discretion of the program director and faculty AND based on the JRCERT recognition process. Each student has access to clinical facilities that offer a balanced education sufficient in quantity and variety of MRI examinations as well as diversified modern equipment. A standardized evaluation system is followed through documentation of a student’s clinical progress for the purpose of providing developmental assistance in correcting weaknesses. All students are required to demonstrate their competence in a variety of procedures and tasks. School faculty makes every effort to preserve educational cohesiveness without compromising the patient care responsibility of the Magnetic Resonance Imaging department. The program faculty schedules each student to practice individually with registered MRI technologists to ensure close direct or indirect supervision and to permit the student to obtain more than ample experience in all practical phases of routine, specialized, and emergency clinical functions. A 1:1 student to magnet ratio is maintained at all times. Clinical schedules are posted by the Educational Coordinator. The program faculty has the right to make changes to the clinical assignment schedule if deemed necessary or advantageous. A student will never be expected to replace a registered technologist.
Sample 1
Clinical Practicum. The required clinical practicum is referred to as competency-based education. The curriculum is structured based on defined objectives and competencies. Clinical education is a planned and structured experience. The 20-month training program is an inter-sequential integration of didactic and practical learning through classroom lectures, clinical laboratories, supplementary lectures, discussions, demonstrations, and supervised practice of standardized procedures. All clinical affiliates offer a balanced education sufficient in quantity and variety of general radiography examinations as well as diversified modern equipment. All students will have an opportunity to observe in interventional radiography, radiation therapy, nuclear medicine technology, computed tomography, diagnostic medical sonography, and magnetic resonance imaging. A standardized evaluation system is followed to document the student’s clinical progress throughout the program. All students are required to demonstrate competence in a variety of procedures and tasks. School faculty makes every effort to preserve educational cohesiveness without compromising the patient care responsibilities of the department. The program faculty has the right to make changes to the clinical assignment schedule if deemed necessary or advantageous. A student will never be expected to replace the registered technologist. CLINICAL SCHEDULE Students will be scheduled at a specific clinical site. The schedule will be given in advance so students can plan accordingly. The rotations will be equally distributed. Changes can be made by program faculty due to extenuating circumstances. CLINICAL SUPERVISION Program faculty schedules each student to practice individually with a certified radiologic technologist (RT) to ensure direct or indirect supervision. Direct Supervision An RT is present in the x-ray room during student performance of a procedure or task. The RT will assess patient condition in relation to student knowledge and assist as needed throughout the exam. Direct supervision is required: ▪ Until the student proves competent on a particular procedure or task ▪ During performance of a competency evaluation ▪ During repeat images ▪ During RIMI rotations
Sample 1
Clinical Practicum. School is committed to excellence by meeting the educational needs of students and the healthcare community. School shall be responsible for the development, implementation, and operation of the clinical component of its educational programs offered and conducted at the Facility pursuant to this Agreement (collectively referred to herein as the “Practicum”). Such responsibilities of School include the following:
Sample 1
Clinical Practicum. During the clinical rotation training experiences, students perform hands-on advanced clinical training tasks under the supervision of an on-site clinical preceptor. The MLS Program and the student work together in identifying an appropriate clinical laboratory that will serve as a clinical training site. In some cases, more than one clinical training site may be needed to ensure all required competencies are taught and assessed. Training usually occurs on the first shift. Students may need to revise their work schedule or take time-off to complete clinical hours. Admission Period: Northeast Mississippi Community College students must be admitted to the UC College of Allied Health Sciences during the duration of this agreement (i.e. between September 2022 and August 2025). Agreement Execution Date: September 2022 Agreement End Date: August 2025 TRANSFER ARTICULATION AGREEMENT Northeast Mississippi Community College, Associate of Applied Science, Medical Laboratory Technology to University of Cincinnati, College of Allied Health Sciences, Bachelor of Science, Medical Laboratory Science (ONLINE)
Sample 1
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Related to Clinical Practicum

  • Part 2 – Medical Practitioner please complete the following

  • Professional Practice The parties agree that nurses who have professional practice complaints will make such complaint in writing to their manager and if such complaint is not resolved then it will be considered an appropriate topic at ONA management committee, unless otherwise agreed by the parties. The parties agree that ONA members may use the ONA Professional Responsibility and Workload Report Form.

  • Commercial Practices Borrower assumes all risks of the acts or omissions of any LC Beneficiary or transferees of any Letter of Credit with respect to the use of such Letter of Credit. Borrower agrees that neither any LC Issuing Bank, Administrative Agent nor any Lender (nor any of their respective directors, officers, or employees) shall be liable or responsible for: (a) the use which may be made of any Letter of Credit or for any acts or omissions of any LC Beneficiary or transferee in connection therewith; (b) any reference which may be made to this Agreement or to any Letter of Credit in any agreements, instruments or other documents; (c) the validity, sufficiency or genuineness of documents other than the Letters of Credit, or of any endorsement(s) thereon, even if such documents should in fact prove to be in any or all respects invalid, insufficient, fraudulent or forged or any statement therein proved to be untrue or inaccurate in any respect whatsoever; (d) payment by any LC Issuing Bank against presentation of documents which do not strictly comply with the terms of the applicable Letter of Credit, including failure of any documents to bear any reference or adequate reference to such Letter of Credit; or (e) any other circumstances whatsoever in making or failing to make payment under any Letter of Credit, except only that an LC Issuing Bank shall be liable to Borrower for acts or events described in clauses (a) through (e) above, to the extent, but only to the extent, of any direct damages, as opposed to indirect, special or consequential damages, suffered by Borrower which Borrower proves were caused by (i) any LC Issuing Bank’s willful misconduct or gross negligence in determining whether a drawing made under the applicable Letter of Credit complies with the terms and conditions therefor stated in such Letter of Credit or (ii) any LC Issuing Bank’s willful failure to pay under any Letter of Credit after a drawing by the respective LC Beneficiary strictly complying with the terms and conditions of the applicable Letter of Credit. Without limiting the foregoing, any LC Issuing Bank may accept any document that appears on its face to be in order, without responsibility for further investigation. Borrower hereby waives any right to object to any payment made under a Letter of Credit with regard to a drawing that is in the form provided in such Letter of Credit but which varies with respect to punctuation (except punctuation with respect to any Dollar amount specified therein), capitalization, spelling or similar matters of form.

  • Clinical 2.1 Provides comprehensive evidence based nursing care to patients including assessment, intervention and evaluation.

  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMEA, Health Canada and other comparable drug and medical device (including diagnostic product) regulatory agencies outside of the United States to which they are subject; the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Disclosure Package and the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement, the Time of Sale Disclosure Package or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMEA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.

  • Research Project 3.1 These Materials and Data will be used by Recipient's PI solely in connection with the Research Project, as named and described in the attached research application (insert Research Project name below):

  • 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.

  • Professional Practices All professional services to be provided by Consultant pursuant to this Agreement shall be provided by personnel experienced in their respective fields and in a manner consistent with the standards of care, diligence and skill ordinarily exercised by professional consultants in similar fields and circumstances in accordance with sound professional practices. Consultant also warrants that it is familiar with all laws that may affect its performance of this Agreement and shall advise City of any changes in any laws that may affect Consultant’s performance of this Agreement.

  • Development Activities The Development activities referred to in item “b” of paragraph 3.1 include: studies and projects of implementation of the Production facilities; drilling and completion of the Producing and injection xxxxx; and installation of equipment and vessels for extraction, collection, Treatment, storage, and transfer of Oil and Gas. The installation referred to in item “c” includes, but is not limited to, offshore platforms, pipelines, Oil and Gas Treatment plants, equipment and facilities for measurement of the inspected Production, wellhead equipment, production pipes, flow lines, tanks, and other facilities exclusively intended for extraction, as well as oil and gas pipelines for Production Outflow and their respective compressor and pumping stations.

  • Project Initiation i - Upon final execution of the Agreement with the DISTRICT, the ARCHITECT shall: ♦ Review the Program Management Plan (PMP) with the DISTRICT and its representatives to familiarize them with the proposed tasks and schedule and develop necessary modifications. The PMP defines the Program Master Schedule and Budgets and each Project scope and budget.

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