Clinical Advisory Groups (CAGs) definition

Clinical Advisory Groups (CAGs) means groups that are composed of individuals with clinical or industry experience and knowledge of specific care or conditions. The CAGs review clinical and episodic bundles, subpopulations and outcome measures that are relevant to the New York State Medicaid Program and make recommendations to SDOH for inclusion in the CAG Playbooks.
Sample 1

Examples of Clinical Advisory Groups (CAGs) in a sentence

  • The PLAC will initiate and receive referrals of PLAC business with the Clinical Advisory Groups (CAGs), the Panel of Clinical Experts (Panel), Health Economics Sub-Committee (HESC), the Therapeutic Goods Administration (TGA), Medical Services Advisory Committee (MSAC), and the Pharmaceutical Benefits Advisory Committee (PBAC).

  • Attachment A - Nominee and Member Risk Assessment Matrix 9 Purpose The purpose of this document is to set out the arrangements under which the Clinical Advisory Groups (CAGs) will operate to deliver on their Terms of Reference.

  • In making recommendations, the PLAC considers advice from Clinical Advisory Groups (CAGs) and members of the Panel of Clinical Experts (PoCE).

  • The Prostheses List Advisory Committee We would question the purpose of the PLAC and its Clinical Advisory Groups (CAGs).

  • The quality standards that have been considered by the Clinical Advisory Groups (CAGs) have been drawn from a range of national and regional documents and reports, for example Standards for Maternity Care (RCOG 2008) and Clinical Negligence Scheme for Trusts Maternity Standards 2012/13, and outputs from the North East Clinical Innovation Teams.

  • The purpose of this document is to set out the arrangements under which the Clinical Advisory Groups (CAGs) will operate to deliver on their Terms of Reference.

  • The state Department of Health (DOH) has posted the Value Based Payment (VBP) Clinical Advisory Groups (CAGs) Recommendation Reports for Chronic Heart Disease; Pulmonary; and Diabetes.

  • P4R).* Final Workgroup approval will occur annually in September/ October Quality Measure Categorization• Category 1 and 2 quality measures are recommended by the Clinical Advisory Groups (CAGs), accepted bythe State, and approved by the VBP Workgroup.The State classified each Category 1 measure as P4P or P4R:• At least one Category 1 P4P measure must be included in a VBP contract.

  • In order to add or update an item on the PL, a ‘sponsor’ (the medical device company who owns the new technology) must submit an application, which is assessed by the PLAC’s associated Clinical Advisory Groups (CAGs) to determine suitability of the device for inclusion on the list.

  • These roles are now performed by the Prostheses List Advisory Committee (PLAC) and its subcommittees, such as the Clinical Advisory Groups (CAGs) and Panels of Clinical Experts.

Related to Clinical Advisory Groups (CAGs)

  • Technical Advisory Committee means the external committee to be established and appointed by the Steering Committee to provide technical input for decisions to be taken by the Steering Committee; and

  • 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.

  • Medical Advisory Committee means the Medical Advisory Committee established by the Board as required by the Public Hospitals Act;

  • Advisory Group has the meaning set forth in Section 9.14(c).

  • Medical Advise means any consultation or advice from a Medical Practitioner including the issue of any prescription or repeat prescription.

  • 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.

  • 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.

  • clinical evidence means clinical data and clinical evaluation results pertaining to a device of a sufficient amount and quality to allow a qualified assessment of whether the device is safe and achieves the intended clinical benefit(s), when used as intended by the manufacturer;

  • Drug therapy management means the review of a drug therapy regimen of a patient by one or more pharmacists for the purpose of evaluating and rendering advice to one or more practitioners regarding adjustment of the regimen.

  • Medical evaluation means the process of assessing an individual's health status that includes a medical history and a physical examination of an individual conducted by a licensed medical practitioner operating within the scope of his license.

  • Stationary beam radiation therapy means radiation therapy without displacement of one or more mechanical axes relative to the patient during irradiation.

  • OPSI Advisory Committee means the committee established under Tariff, Attachment M, section III.G.

  • continuing professional development means the continuing professional development contemplated in section 32;

  • 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.

  • Monitoring Committee means the committee established under clause 10 of this Award.

  • 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;

  • District Evaluation Advisory Committee means a group created to oversee and guide the planning and implementation of the Board of Education's evaluation policies and procedures as set forth in N.J.A.C. 6A:10-2.3.

  • Medical Affairs Activities means, with respect to any country or other jurisdiction in the Territory, the coordination of medical information requests and field based medical scientific liaisons with respect to Licensed Compounds or Licensed Products, including activities of medical scientific liaisons and the provision of medical information services with respect to a Licensed Compound or Licensed Product.

  • Joint Commercialization Committee or “JCC” has the meaning set forth in Section 3.4 (Joint Commercialization Committee).

  • Participating Clinical Professional Counselor means a Clinical Professional Counselor 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.

  • Background radiation means radiation from cosmic sources; naturally occurring radioactive materials, including radon (except as a decay product of source or special nuclear material); and global fallout as it exists in the environment from the testing of nuclear explosive devices or from past nuclear accidents such as Chernobyl that contribute to background radiation and are not under the control of the licensee. “Background radiation” does not include sources of radiation from radioactive materials regulated by the agency.

  • Technical Committee means the body established in accordance with article VII;

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Nuclear fuel cycle-related research and development activities means those activities which are specifically related to any process or system development aspect of any of the following: - conversion of nuclear material, - enrichment of nuclear material, - nuclear fuel fabrication, - reactors, - critical facilities, - reprocessing of nuclear fuel, - processing (not including repackaging or conditioning not involving the separation of elements, for storage or disposal) of intermediate or high-level waste containing plutonium, high enriched uranium or uranium-233, but do not include activities related to theoretical or basic scientific research or to research and development on industrial radioisotope applications, medical, hydrological and agricultural applications, health and environmental effects and improved maintenance.

  • Multiphase professional services contract means a contract for the providing of professional