Clinical Establishment Rules definition

Clinical Establishment Rules means The West Bengal Clinical Establishment Rules 2003 and amended time to time.
Clinical Establishment Rules means The West Bengal Clinical Establishment Rules 2003 or modified hereafter.

Examples of Clinical Establishment Rules in a sentence

  • Secondly, by closely centering the development trend of intelligent equipment manufacturing, the Company intensified scientific and technological innovation, took the initiative to extend industrial chains, strengthened the integration of service, promoted the comprehensive value and competitive advantages of products and services and strived for more shares in the limited market.

  • The Hospital Authority has on the date hereof handed over to the Concessionaire physical possession of the Hospital Site as described under Schedule “A” as per the applicable norms of The Clinical Establishment Acts and The Clinical Establishment Rules free from Encumbrance along with all the equipments and accessories described under Schedule “B” installed in the hospital site for operation and management of the Dialysis Services.

  • The Private Service Provider will comply with all statutory requirements as applicable under Xxx Xxxx Xxxxxx Xxxxxxxx Xxxxxxxxxxxxx Xxx 0000 and The West Bengal Clinical Establishment Rules 2003 as amended hereafter and other applicable Acts and Laws.

  • The Hospital Authority has on the date hereof handed over to the Concessionaire physical possession of the Hospital Site as described under Schedule “A” as per the applicable norms of The Clinical Establishment Acts and The Clinical Establishment Rules free from Encumbrance along with all the equipments and accessories described under Schedule “B” installed in the hospital site for operation and management of the Digital X-Ray services.

  • The Hospital / Diagnostic Centre shall submit an annual report in Form No V and VI as per provision of the West Bengal Clinical Establishment Rules, 2003 to the licensing authority.

  • The desirability of the employer in selecting candidates by virtue of the said advertisement was that the candidates should have one year training after acquiring diploma in laboratory technology recognized by Government of West Bengal, in any government hospital or in a clinical establishment licensed under the West Bengal Clinical Establishment Rules, 2003 or a post graduate diploma in laboratory technology from any recognized university.

Related to Clinical Establishment Rules

  • educational establishment means any school, college or other educational body designated by the Minister by order either specifically or by reference to a class, for the purposes of this Act;

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Commercial establishment means a place of business which is at all times equipped with sufficient tables and seats to accommodate twenty-five persons at one time, and the licensed premises of which conform to the standards and specifications of the division.

  • Cannabis production establishment agent means a cannabis cultivation facility

  • Clinical peer means a physician or other health care professional who holds a non-restricted license in a state of the United States and in the same or similar specialty as typically manages the medical condition, procedure or treatment under review.

  • Step therapy protocol means a protocol or program that establishes the specific

  • Project Implementation Plan means the detail plan submitted by the Developer with regard to development of Project Facilities and its operation and management thereof in accordance with this Agreement and to be appended as Schedule 9 to this Agreement.

  • Objective medical evidence means reports of examinations or treatments; medical signs which are anatomical, physiological, or psychological abnormalities that can be observed; psychiatric signs which are medically demonstrable phenomena indicating specific abnormalities of behavior, affect, thought, memory, orientation, or contact with reality; or laboratory findings which are anatomical, physiological, or psychological phenomena that can be shown by medically acceptable laboratory diagnostic techniques, including but not limited to chemical tests, electrocardiograms, electroencephalograms, X-rays, and psychological tests;

  • Cannabis production establishment agent registration card means a registration card that the department issues that:

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Clinical Trials means a controlled study in humans of the safety or efficacy of a Product, and includes, without limitation, such clinical trials as are designed to support expanded labeling or to satisfy the requirements of an Agency in connection with any Product Approval and any other human study used in research and Development of a Product.

  • Development Plan has the meaning set forth in Section 3.2.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Commercialization Plan has the meaning set forth in Section 6.2.

  • Quality Assurance Program means the overall quality program and associated activities including the Department’s Quality Assurance, Design-Builder Quality Control, the Contract’s quality requirements for design and construction to assure compliance with Department Specifications and procedures.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Development Consent means the consent granted to the Development Application for the Development and includes all modifications made under section 4.55 of the Act.

  • Project Implementation Manual or “PIM” means the manual setting out the measures required for the implementation of the Project, as the same may be amended from time to time, subject to prior approval of the Association;

  • Clinical review criteria means the written screening procedures, decision abstracts, clinical protocols, and practice guidelines used by a health carrier to determine the necessity and appropriateness of health care services.

  • Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Quality Management Plan means the portion of the Project Development Plan providing the information requested in Section 4.3 of Exhibit B to the ITP.

  • Quality Management System means a set of interrelated or interacting elements that organisations use to direct and control how quality policies are implemented and quality objectives are achieved;

  • Clinical Trial means any human clinical trial of a Product.

  • Phase 2 Clinical Trial means a human clinical trial, for which the primary endpoints include a determination of dose ranges or an indication of efficacy in patients being studied as described in 21 C.F.R. §312.21(b), or an equivalent clinical trial in a country in the Territory other than the United States.