MHLA Clinic definition

MHLA Clinic means any clinic contracted with County to provide primary and ancillary care services through the MHLA Program.

Examples of MHLA Clinic in a sentence

  • County will make the final decision regarding the appropriate action needed.7.6 Contractor shall provide independent 340B audits consistent with HRSA regulations for each 340B Contract Pharmacy relationship except for those MHLA Clinic on-site 340B Contract Pharmacies.

  • DHS Central Pharmacy medications will be mailed directly to Patient or MHLA Clinic via the Department of Health Services (DHS) Specialty Pharmacy, which will be a contracted pharmacy that is approved under HRSA's 340B Drug Pricing Program.

  • The DHS Specialty Pharmacy and on-site and other HRSA-approved MHLA Clinic designated 340B Contract Pharmacies will be included within the Contract Pharmacy Network upon County approval.

  • In addition, the MHLA Pharmacy Services Program will be allowing approved MHLA Clinic dispensaries to dispense medications directly to patients.

  • Attachment II provides the data that MHLA Clinic dispensaries will transmit to Contractor.

  • BackgroundAn early use of the term “ontology” was in philosophy (Wolffe, C., Philosophia Prima Sive Ontologia, 1729) where its use means “a branch of metaphysics relating to the nature and relations of being.” Computational scientist’s adopted the general meaning of the term to be the “relations of being” for describing how data is related.

  • FIRM FIXED PRICE Contract Line No. (CLIN) Item Description COST REIMBURSEMENT Contract Line No. (CLIN)Item DescriptionNot-to-Exceed Amount B.3.1 District estimate for the project ranges of $80,000 to $100,000 and includes all pricing components.

  • Contractor shall provide medication dispensary data from approved MHLA Clinic dispensaries in NCPDP format to County within 1 business day upon receipt from MHLA dispensaries.

Related to MHLA 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.

  • 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.

  • veterinary clinic means a building where animals are given medication or surgical treatment and are cared for during the time of such treatment for financial gain;

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Hospital clinic means an outpatient care clinic operated and affiliated with a hospital and under the direct authority of the hospital’s P&T committee.

  • 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.

  • Health screening means the use of one or more diagnostic tools to test a person for the presence or precursors of a particular disease.

  • Non-Participating Clinical Laboratory means a Clinical Laboratory which does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan provide services to you at the time services are rendered.

  • 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.

  • Non-Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who does not have 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.

  • 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:

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

  • Approved abuse education training program means a training program using a curriculum approved by the abuse education review panel of the department of public health or a training program offered by a hospital, a professional organization for physicians, or the department of human services, the department of education, an area education agency, a school district, the Iowa law enforcement academy, an Iowa college or university, or a similar state agency.

  • Child Care Program means a person or business that offers child care.

  • 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.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Participating Clinical Social Worker means a Clinical Social Worker 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.

  • 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.

  • cGCP means the then current Good Clinical Practices that establish the national and international ethical and scientific quality standards for designing, conducting, recording and reporting clinical trials that are promulgated or endorsed for the United States by the FDA (including through ICH E6 and 21 CFR Parts 50, 54, 56 and 312) and for outside the United States by comparable Governmental Authorities.

  • PDMA means the Prescription Drug Marketing Act of 1987, as amended from time to time, together with any rules or regulations promulgated thereunder.

  • 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.

  • Participating Retail Health Clinic means a Retail Health Clinic 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.

  • Federal Health Care Program has the meaning set forth in 42 U.S.C. 1320a-7b(f).

  • Health Canada means the Canadian federal Department of Health and any successor thereof.

  • PMDA means Japan’s Pharmaceuticals and Medical Devices Agency and any successor agency(ies) or authority having substantially the same function.

  • MFDA means the Mutual Fund Dealers Association of Canada;