LFP Clinic definition

LFP Clinic means a medical clinic in which a physician enrolled in the LFP Payment Model regularly provides Community Longitudinal Family Physician Services.
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LFP Clinic means a medical clinic in which a physician enrolled in the LFP Payment Model regularly provides Community Longitudinal Family Physician Services. (q) “LFP Host Physician” means a physician who is enrolled in the LFP Payment Model and having another physician substitute for them on a temporary basis while they are away from their practice.
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Examples of LFP Clinic in a sentence

  • This requirement is regardless of whether the service is provided at the LFP Clinic or at another location.For individual services, physicians must provide the actual start and end time on the claim.

  • For clarity, if a physician provides Indirect Patient Care for a patient located at a Facility while the physician is between patient interactions in the course of their workday at an LFP Clinic, this Indirect Patient Care time is payable under the LFP Payment Model.

  • Such expenses incurred outside Canada on an elective basis are not payable.

  • If a physician practices at multiple LFP Clinic locations, submit a separate Transition Code with the associated MSP Facility Number of each LFP Clinic location where they meet the eligibility criteria and provide the Required Services.

  • A physician submits the Transition Code after the Registration Code using their MSP Practitioner Number and the following “patient” demographic information:• PHN: 9753035697• Patient Surname: Portal• First name: GPSC• Date of Birth: January 1, 2013• ICD-9 code: L23 The Transition Code must be submitted using the MSP Facility Number associated with the LFP Clinic.

  • Payable for an in-person interaction provided in an LFP Clinic or Maternity Clinic.

  • Unless CPSBC guidance on the appropriate use of virtual care states otherwise, the physician must provide both in-person and virtual visits to patients in their LFP Clinic.

  • A physician submits the Transition Code after the Registration Code using their MSP Practitioner Number and the following “patient” demographic information:• PHN: 9753035697• Patient Surname: Portal• First name: GPSC• Date of Birth: January 1, 2013• ICD-9 code: L23 The Transition Code must be submitted using the Facility Number associated with the LFP Clinic.

  • The Assignee may take or release other security, may release any party primarily or secondarily liable for any of the Liabilities, may grant extensions, renewals or indulgences with respect to the Liabilities, or may apply to the Liabilities in such order as the Assignee shall determine, the proceeds of the Policy hereby assigned or any amount received on account of the Policy by the exercise of any right permitted under this assignment, without resorting or regard to other security.

  • An LFP Locum must may bill Locum Time Codes and Locum Patient Interaction Codes for LFP Locum Services at a Host Physician’s longitudinal family medicine clinic LFP Clinic or Host Physician’s Maternity Clinic.

Related to LFP Clinic

  • Rural health clinic means a rural health clinic as defined under section 1861 of part C of title XVIII of the social security act, chapter 531, 49 Stat. 620, 42 U.S.C. 1395x, and certified to participate in medicaid and medicare.

  • HITECH means the Health Information Technology for Economic and Clinical Health Act.

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • 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.

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Phase I Clinical Trial means a study in humans which provides for the first introduction into humans of a product, conducted in normal volunteers or patients to generate information on product safety, tolerability, pharmacological activity or pharmacokinetics, or otherwise consistent with the requirements of U.S. 21 C.F.R. §312.21(a) or its foreign equivalents.

  • GCP means good clinical practices, which are the then-current standards for Clinical Trials for pharmaceuticals, as set forth in the FD&C Act or other Applicable Law, and such standards of good clinical practice as are required by the Regulatory Authorities of Europe and other organizations and governmental authorities in countries for which the applicable Licensed Agent or Product is intended to be Developed, to the extent such standards are not less stringent than United States standards.